Canonical Allele Identifier: PA2828475005
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 392633

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358176.1:p.Trp923Arg
CA16603904
NM_001371247.1:c.2767T>C
CA349015396
NM_001371247.1:c.2767T>A