Canonical Allele Identifier: PA645492790
Gene: ROR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 367501

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004551.2:p.Val574Leu
CA5120595
NM_004560.4:c.1720G>T
CA373797710
NM_004560.4:c.1720G>C