Canonical Allele Identifier: PA2828474694
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 207072

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358176.1:p.Ser686Ile
CA318168
NM_001371247.1:c.2057G>T