Canonical Allele Identifier: PA2825941561
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1371156
ClinVar RCV Id: RCV003772616
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Asp1113Tyr
CA352138697
NM_001160160.2:c.3337G>T