Canonical Allele Identifier: PA284930
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68531
ClinVar RCV Id: RCV000059404 RCV001344646
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008851.3:p.Gly1222Arg
CA284928
NM_006920.6:c.3664G>C