Canonical Allele Identifier: PA173327
Gene: ROR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 159817
ClinVar RCV Id: RCV000147388 RCV000180603 RCV000337021 RCV000398258
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004551.2:p.Ser762Leu
CA173326
NM_004560.4:c.2285C>T