Canonical Allele Identifier: PA2827923583
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67939

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Arg1613His
CA018735
NM_001354701.2:c.4838G>A