Canonical Allele Identifier: PA314959
Gene: GRIN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 205663
ClinVar RCV Id: RCV000187649

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000824.1:p.Met932Ile
CA314958
NM_000833.5:c.2796G>C
CA394709339
NM_000833.5:c.2796G>T
CA394709340
NM_000833.5:c.2796G>A