Canonical Allele Identifier: PA2825130879
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 924568
ClinVar RCV Id: RCV001843271

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Val1172Ile
CA352138289
NM_000335.5:c.3514G>A