Canonical Allele Identifier: PA173319
Gene: ROR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 159813
ClinVar RCV Id: RCV000147384 RCV000171424 RCV001353137
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004551.2:p.Arg657His
CA173318
NM_004560.4:c.1970G>A