Canonical Allele Identifier: PA2499239129
Gene: GRIN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1053271
ClinVar Variation Id: 1479761
ClinVar RCV Id: RCV002009886

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001127880.1:p.Ser24Arg
CA7897052
NM_001134408.2:c.72C>G
CA394715784
NM_001134408.2:c.72C>A
CA394715788
NM_001134408.2:c.70A>C