Canonical Allele Identifier: PA2825128832
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 926252
ClinVar RCV Id: RCV001841051

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Val300Asp
CA352150387
NM_000335.5:c.899T>A