Canonical Allele Identifier: PA645492301
Gene: ROR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 367507
ClinVar RCV Id: RCV000360660 RCV000308020 RCV002058818 RCV002524607
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004551.2:p.Ala436Val
CA5120732
NM_004560.4:c.1307C>T