Canonical Allele Identifier: PA645374166
Gene: GRIN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 234730
ClinVar RCV Id: RCV000215426
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000825.2:p.Met157Ile
CA10577451
NM_000834.3:c.471G>C
CA384054731
NM_000834.3:c.471G>T
CA384054733
NM_000834.3:c.471G>A