Canonical Allele Identifier: PA2825945813
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 75052

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Arg1875Cys
CA064797
NM_001160161.2:c.5623C>T