Canonical Allele Identifier: PA2825353527
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 984860

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035232.1:p.Gly211Asp
CA349017386
NM_001040142.2:c.632G>A