Canonical Allele Identifier: PA2825945336
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67939

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Arg1578His
CA018735
NM_001160161.2:c.4733G>A