Canonical Allele Identifier: PA2573184681
Gene: GRIN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1368557
ClinVar RCV Id: RCV001867555
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001127880.1:p.Met39Leu
CA394715701
NM_001134408.2:c.115A>T
CA394715703
NM_001134408.2:c.115A>C