Canonical Allele Identifier: PA2825942322
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67939

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Arg1599His
CA018735
NM_001160160.2:c.4796G>A