Canonical Allele Identifier: PA891848304
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 586499
ClinVar RCV Id: RCV000713077
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066287.2:p.Leu210Arg
CA349017374
NM_021007.3:c.629T>G