Canonical Allele Identifier: PA2573172039
Gene: GRIN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 1386960
ClinVar RCV Id: RCV001881711

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000825.2:p.Leu62Pro
CA6461448
NM_000834.3:c.185T>C