Canonical Allele Identifier: PA2827921939
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 919359

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Gly538Asp
CA058388
NM_001354701.2:c.1613G>A