Canonical Allele Identifier: PA1139686390
Gene: GRIN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 833834
ClinVar RCV Id: RCV001034341
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001127880.1:p.Met133Val
CA277615495
NM_001134408.2:c.397A>G