Canonical Allele Identifier: PA2825239504
Gene: GRIN2B HGNC NCBI
ClinVar RCV:
RCV002894916
ClinVar Variation:
2038391
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000825.2:p.Asn1365Asp
CA383986623
NM_000834.3:c.4093A>G