Canonical Allele Identifier: PA2825943861
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 201460

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Gly607Asp
CA015379
NM_001160161.2:c.1820G>A