Canonical Allele Identifier: PA891848761
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 567303
ClinVar RCV Id: RCV000687341 RCV002283507
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008851.3:p.Ala104Asp
CA349077094
NM_006920.6:c.311C>A