Canonical Allele Identifier: PA2826984985
Gene: ROR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 594282
ClinVar RCV Id: RCV000729540
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305133.1:p.Thr78Arg
CA373840903
NM_001318204.2:c.233C>G