Canonical Allele Identifier: PA2825130885
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 406448

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Arg1174His
CA061975
NM_000335.5:c.3521G>A