Canonical Allele Identifier: PA2825131892
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 919932

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Ser1608Leu
CA063800
NM_000335.5:c.4823C>T