Allele Registry

Canonical Allele Identifier: PA173329

Gene: ROR2 HGNC NCBI

ClinVar RCV:

RCV000147389

RCV000344414

RCV000382446

RCV001095340

RCV001522558

ClinVar Variation:

159818

HGVS (amino-acid)	Matching Registered Transcripts
NP_004551.2:p.Val819Ile	CA173328 NM_004560.4:c.2455G>A