Canonical Allele Identifier: PA2499234240
Gene: GRIN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 1060621
ClinVar RCV Id: RCV001370078
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000825.2:p.Phe143Leu
CA6461401
NM_000834.3:c.427T>C
CA384054888
NM_000834.3:c.429C>G
CA384054889
NM_000834.3:c.429C>A