Canonical Allele Identifier: PA265140
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67748

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Arg893Cys
CA016390
NM_000335.5:c.2677C>T