Canonical Allele Identifier: PA308021
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 201579

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Ala665Thr
CA015693
NM_000335.5:c.1993G>A