Canonical Allele Identifier: PA265085
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67732

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Arg814Gln
CA016182
NM_001099404.2:c.2441G>A