Canonical Allele Identifier: PA1139717408
Gene: ROR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 841827

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004551.2:p.Gln850His
CA373793854
NM_004560.4:c.2550G>T
CA373793857
NM_004560.4:c.2550G>C