NM_001025366.2:c.659-99G>A

HGVS Expressions

  • NG_008732.1:g.12155G>A
  • NM_001025366.2:c.659-99G>A
  • NP_001020537.2:p.?
  • NC_000006.12:g.43777370G>A
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Clinvar Clinical Significance

Benign

CTGA Clinical Significance

Association

Variant Type

Substitution

dbSNP

3024997

Clinvar

1233590

Epidemiology in the Arab World

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