Allele Registry

Canonical Allele Identifier: PA248109

Gene: ROR2 HGNC NCBI

ClinVar RCV:

RCV000180607

RCV000660425

RCV002503700

ClinVar Variation:

199098

HGVS (amino-acid)	Matching Registered Transcripts
NP_004551.2:p.Cys694Arg	CA248108 NM_004560.4:c.2080T>C