Canonical Allele Identifier: PA2827923517
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1992327

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Val1578Ala
CA72942393
NM_001354701.2:c.4733T>C