Canonical Allele Identifier: PA2825128122
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 463358

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Arg27Cys
CA056855
NM_000335.5:c.79C>T