Canonical Allele Identifier: PA2825130931
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 2189234

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Val1189Phe
CA352138191
NM_000335.5:c.3565G>T