Canonical Allele Identifier: PA2573181793
Gene: GRIN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1406453
ClinVar RCV Id: RCV001915831

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001127880.1:p.Thr1275Ser
CA394705925
NM_001134408.2:c.3824C>G
CA394705927
NM_001134408.2:c.3823A>T