Canonical Allele Identifier: PA2826985003
Gene: ROR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2387894
ClinVar RCV Id: RCV002698698
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305133.1:p.Arg107Trp
CA5121062
NM_001318204.2:c.319C>T