Canonical Allele Identifier: PA2827922883
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 919433

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Asp1162Tyr
CA72923946
NM_001354701.2:c.3484G>T