NM_000077.4:c.442G>A

HGVS Expressions

  • NG_007485.1:g.28575G>A
  • NM_000077.4:c.442G>A
  • NP_000068.1:p.Ala148Thr
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Genomic Location

chr9:21970917

Clinvar Clinical Significance

Benign

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

dbSNP

3731249

Clinvar

41580

Epidemiology in the Arab World

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