Canonical Allele Identifier: PA2828470266
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1727249
ClinVar RCV Id: RCV002319766
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358175.1:p.Asp12Asn
CA349009717
NM_001371246.1:c.34G>A