Canonical Allele Identifier: PA2825131210
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1098787
ClinVar RCV Id: RCV001420834

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Arg1315Pro
CA352148090
NM_000335.5:c.3944G>C