Canonical Allele Identifier: PA2825496599
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 9376

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Arg1605Gln
CA018670
NM_001099405.2:c.4814G>A