Canonical Allele Identifier: PA248107
Gene: ROR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 159819
ClinVar RCV Id: RCV000147390 RCV000180606 RCV000262682 RCV000513925
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004551.2:p.Asp935Glu
CA248106
NM_004560.4:c.2805C>G
CA5120307
NM_004560.4:c.2805C>A