Canonical Allele Identifier: PA2826260853
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 93661

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001189364.1:p.Pro1984His
CA221611
NM_001202435.3:c.5951C>A