Canonical Allele Identifier: PA2573275659
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1686160
ClinVar RCV Id: RCV002250327
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066287.2:p.Asn212Asp
CA349017397
NM_021007.3:c.634A>G