Canonical Allele Identifier: PA284933
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_008851.3:p.Arg1234Gln
CA284931
NM_006920.6:c.3701G>A