Canonical Allele Identifier: PA2573063739
Gene: GRIN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 1309504
ClinVar RCV Id: RCV001765673

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000825.2:p.Ser305Phe
CA384053164
NM_000834.3:c.914C>T