Canonical Allele Identifier: PA2825538075
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 463304
ClinVar RCV Id: RCV003654421

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Asn598Ser
CA352146132
NM_001099404.2:c.1793A>G