Canonical Allele Identifier: PA354197
Gene: GRIN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 224086
ClinVar RCV Id: RCV000209917 RCV000794240
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000825.2:p.Thr685Pro
CA354196
NM_000834.3:c.2053A>C