Canonical Allele Identifier: PA2826258222
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2898671
ClinVar RCV Id: RCV003753079

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001189364.1:p.Gly232Asp
CA349073897
NM_001202435.3:c.695G>A