Canonical Allele Identifier: PA2825538462
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 940929
ClinVar RCV Id: RCV001586051

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Leu939Pro
CA352140706
NM_001099404.2:c.2816T>C