Canonical Allele Identifier: PA112979
Gene: OTX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 9516
ClinVar RCV Id: RCV000010124
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001257452.1:p.Arg89Gly
CA120500
NM_001270523.2:c.265C>G