Canonical Allele Identifier: PA2825130257
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 940929
ClinVar RCV Id: RCV001586051

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Leu939Pro
CA352140706
NM_000335.5:c.2816T>C