Canonical Allele Identifier: PA2829675778
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 662021
ClinVar RCV Id: RCV000819559

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008851.3:p.Val1286Gly
CA1942867
NM_006920.6:c.3857T>G