Canonical Allele Identifier: PA2825359020
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 206975

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035233.1:p.Gly899Asp
CA317895
NM_001040143.2:c.2696G>A