Canonical Allele Identifier: PA2825129678
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1044880
ClinVar RCV Id: RCV003770995

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Gly652Val
CA352145086
NM_000335.5:c.1955G>T