Canonical Allele Identifier: PA284984
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68554
ClinVar RCV Id: RCV000059428 RCV000584823 RCV000636349
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008851.3:p.Asp1597Tyr
CA284982
NM_006920.6:c.4789G>T