Canonical Allele Identifier: PA2580303509
Gene: ROR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1957900
ClinVar RCV Id: RCV002690977

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004551.2:p.Tyr688Asp
CA5120499
NM_004560.4:c.2062T>G