Canonical Allele Identifier: PA2825357769
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1010462
ClinVar RCV Id: RCV001308099
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035233.1:p.Asn116Ser
CA349011765
NM_001040143.2:c.347A>G