Canonical Allele Identifier: PA2825943951
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 652887

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Arg661Gln
CA72932963
NM_001160161.2:c.1982G>A