Canonical Allele Identifier: PA1139682562
Gene: GRIN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 938350
ClinVar RCV Id: RCV001207551 RCV001760174
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000825.2:p.Pro122Ser
CA384053642
NM_000834.3:c.364C>T