Canonical Allele Identifier: PA330014
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67828
ClinVar RCV Id: RCV000058605
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Ile1278Asn
CA017542
NM_001099404.2:c.3833T>A