Canonical Allele Identifier: PA2825945812
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 179372

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Arg1875His
CA019464
NM_001160161.2:c.5624G>A