Canonical Allele Identifier: PA285005
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_008851.3:p.Met1703Arg
CA285003
NM_006920.6:c.5108T>G