Canonical Allele Identifier: PA307332
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 201461

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Gly607Val
CA015393
NM_001099404.2:c.1820G>T