Canonical Allele Identifier: PA2825943752
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 919359

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Gly538Asp
CA058388
NM_001160161.2:c.1613G>A