Canonical Allele Identifier: PA2826259601
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2581808

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001189364.1:p.Gly1233Ser
CA349055647
NM_001202435.3:c.3697G>A