Canonical Allele Identifier: PA2826258034
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 189862

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001189364.1:p.Pro113Thr
CA303135
NM_001202435.3:c.337C>A