Canonical Allele Identifier: PA2825129992
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 519424

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Arg811His
CA060390
NM_000335.5:c.2432G>A