Canonical Allele Identifier: PA645492138
Gene: ROR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 288137

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004551.2:p.Thr190Ala
CA5120972
NM_004560.4:c.568A>G