Canonical Allele Identifier: PA645374350
Gene: GRIN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 245623
ClinVar RCV Id: RCV000236011
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000825.2:p.Val1430Leu
CA10584419
NM_000834.3:c.4288G>C
CA383985594
NM_000834.3:c.4288G>T