Canonical Allele Identifier: PA2825128078
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 519065

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Arg8Gln
CA056648
NM_000335.5:c.23G>A