Canonical Allele Identifier: PA1139686713
Gene: GRIN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 965049
ClinVar RCV Id: RCV001239408
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001127880.1:p.Arg672Gly
CA394797994
NM_001134408.2:c.2014A>G