Canonical Allele Identifier: PA2825128250
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1437736

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Tyr68Cys
CA352158178
NM_000335.5:c.203A>G