Canonical Allele Identifier: PA284855
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68499
ClinVar RCV Id: RCV000059371 RCV001257271 RCV001753478
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008851.3:p.Arg356Gly
CA284853
NM_006920.6:c.1066A>G