Canonical Allele Identifier: PA248109
Gene: ROR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 199098

Amino-acid Alleles

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