Canonical Allele Identifier: PA315082
Gene: GRIN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 205727
ClinVar RCV Id: RCV000187715
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000825.2:p.Val42Ala
CA315081
NM_000834.3:c.125T>C