Canonical Allele Identifier: PA2825944789
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 646267

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Val1233Ala
CA352148254
NM_001160161.2:c.3698T>C