Canonical Allele Identifier: PA2825941089
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 519424
ClinVar RCV Id: RCV000621795 RCV002506507 RCV003542307
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Arg811His
CA060390
NM_001160160.2:c.2432G>A