Canonical Allele Identifier: PA2826013020
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68533
ClinVar RCV Id: RCV000059406 RCV000636387 RCV000188926 RCV001836729
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159436.1:p.Arg1217Gln
CA284931
NM_001165964.3:c.3650G>A