Canonical Allele Identifier: PA2580445949
Gene: OPTN HGNC NCBI

Linked Data

ClinVar Variation Id: 2078827
ClinVar RCV Id: RCV002988839
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_068815.2:p.Met65Thr
CA376027358
NM_021980.4:c.194T>C