Canonical Allele Identifier: PA2825945450
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 9383

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Ser1656Leu
CA018910
NM_001160161.2:c.4967C>T