Canonical Allele Identifier: PA308003
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 201576

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Arg569Gly
CA015193
NM_000335.5:c.1705C>G