Canonical Allele Identifier: PA2825130734
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1371156
ClinVar RCV Id: RCV003772616

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Asp1113Tyr
CA352138697
NM_000335.5:c.3337G>T