Canonical Allele Identifier: PA265084
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67732

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Arg814Gln
CA016182
NM_000335.5:c.2441G>A