Canonical Allele Identifier: PA2825537700
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 532098
ClinVar RCV Id: RCV003539997

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Arg282Gly
CA352150552
NM_001099404.2:c.844C>G