Canonical Allele Identifier: PA2741835329
Gene: GRIN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 2811707
ClinVar RCV Id: RCV003741727

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001127880.1:p.Asn693Lys
CA394797853
NM_001134408.2:c.2079C>G
CA394797854
NM_001134408.2:c.2079C>A