Canonical Allele Identifier: PA2826259184
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 189961

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001189364.1:p.Arg931Pro
CA303413
NM_001202435.3:c.2792G>C