Canonical Allele Identifier: PA2825497192
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 201539

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Ala1810Thr
CA019290
NM_001099405.2:c.5428G>A