Canonical Allele Identifier: PA1139683257
Gene: GRIN2B HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000825.2:p.Ser1043Ala
CA383990789
NM_000834.3:c.3127T>G