Canonical Allele Identifier: PA2825129383
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 919359

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Gly538Asp
CA058388
NM_000335.5:c.1613G>A