Canonical Allele Identifier: PA2825944725
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1305091
ClinVar RCV Id: RCV001773801

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Tyr1187Cys
CA352149290
NM_001160161.2:c.3560A>G