Canonical Allele Identifier: PA2741928945
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2898671
ClinVar RCV Id: RCV003753079

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008851.3:p.Gly232Asp
CA349073897
NM_006920.6:c.695G>A