Canonical Allele Identifier: PA108011
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68564
ClinVar RCV Id: RCV000059439
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.Met1714Arg
CA285003
NM_001165963.4:c.5141T>G