Canonical Allele Identifier: PA2827921340
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1332491
ClinVar RCV Id: RCV001842212

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Tyr112Cys
CA061680
NM_001354701.2:c.335A>G