Canonical Allele Identifier: PA2828473954
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1317603
ClinVar RCV Id: RCV001768169 RCV001868718
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358176.1:p.Ser249Thr
CA349017918
NM_001371247.1:c.745T>A