Allele Registry

Canonical Allele Identifier: PA173327

Gene: ROR2 HGNC NCBI

ClinVar RCV:

RCV000147388

RCV000180603

RCV000337021

RCV000398258

ClinVar Variation:

159817

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