Canonical Allele Identifier: PA284927
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68530
ClinVar RCV Id: RCV000059403 RCV000818870 RCV002054912
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008851.3:p.Leu1196Pro
CA284925
NM_006920.6:c.3587T>C