Canonical Allele Identifier: PA2825217932
Gene: OXTR HGNC NCBI

Linked Data

ClinVar Variation Id: 1221201
ClinVar RCV Id: RCV001597390
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000907.2:p.Ala218Thr
CA2236552
NM_000916.4:c.652G>A