Canonical Allele Identifier: PA2825128705
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1171282
ClinVar RCV Id: RCV001842071

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Leu243Val
CA352150995
NM_000335.5:c.727C>G