Canonical Allele Identifier: PA285071
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68593
ClinVar RCV Id: RCV000059469 RCV000591357 RCV000798343
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008851.3:p.Arg851Gln
CA285069
NM_006920.6:c.2552G>A