Canonical Allele Identifier: PA284978
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68551
ClinVar RCV Id: RCV000059425 RCV001069069 RCV001249684
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008851.3:p.Ile1534Val
CA284976
NM_006920.6:c.4600A>G