Canonical Allele Identifier: PA1139686699
Gene: GRIN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 870418
ClinVar RCV Id: RCV001089991
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001127880.1:p.Ala647Ser
CA394799332
NM_001134408.2:c.1939G>T