Canonical Allele Identifier: PA2825130955
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1172206

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Glu1202Ala
CA352138102
NM_000335.5:c.3605A>C