Canonical Allele Identifier: PA330299
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 68033

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Arg225Gln
CA019719
NM_000335.5:c.674G>A