NM_004304.5:c.4211T>C

HGVS Expressions

  • NG_009445.1:g.732691T>C
  • NM_004304.5:c.4211T>C
  • NP_004295.2:p.Leu1404Pro
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Genomic Location

chr2:29193876

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

Clinvar

645717

Epidemiology in the Arab World

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