Canonical Allele Identifier: PA266125
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68653
ClinVar RCV Id: RCV000059533
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008851.3:p.Asp1731Gly
CA266123
NM_006920.6:c.5192A>G