Canonical Allele Identifier: PA2828473854
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 586499
ClinVar RCV Id: RCV000713077

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358176.1:p.Leu210Arg
CA349017374
NM_001371247.1:c.629T>G