Canonical Allele Identifier: PA2825945493
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 191499

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Ser1684Phe
CA018989
NM_001160161.2:c.5051C>T