Canonical Allele Identifier: PA307923
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 68027

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Arg2012Cys
CA019612
NM_001099404.2:c.6034C>T