Canonical Allele Identifier: PA2825131858
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1992327

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Val1596Ala
CA72942393
NM_000335.5:c.4787T>C