Canonical Allele Identifier: PA2825944604
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 919433

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Asp1109Tyr
CA72923946
NM_001160161.2:c.3325G>T