Canonical Allele Identifier: PA2825537463
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1437736

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Tyr68Cys
CA352158178
NM_001099404.2:c.203A>G