Canonical Allele Identifier: PA2825490213
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 2584499

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Lys1477Thr
CA352145222
NM_001099404.2:c.4430A>C