Canonical Allele Identifier: PA2825941720
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 993536
ClinVar RCV Id: RCV001812342
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Phe1212Val
CA352138031
NM_001160160.2:c.3634T>G