Canonical Allele Identifier: PA284903
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68520
ClinVar RCV Id: RCV000059392 RCV000255485 RCV000763463 RCV000695650
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008851.3:p.Tyr84Cys
CA284901
NM_006920.6:c.251A>G