Canonical Allele Identifier: PA145238
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68512
ClinVar RCV Id: RCV000180909 RCV000059384
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008851.3:p.Ser626Gly
CA145235
NM_006920.6:c.1876A>G