Canonical Allele Identifier: PA254774
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 9382

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Tyr1794_Glu1795insAsp
CA025554
NM_000335.5:c.5382_5384dup