Canonical Allele Identifier: PA2825493421
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 919359

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Gly538Asp
CA058388
NM_001099405.2:c.1613G>A