Canonical Allele Identifier: PA2825537526
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1332491
ClinVar RCV Id: RCV001842212

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Tyr112Cys
CA061680
NM_001099404.2:c.335A>G