Allele Registry

Canonical Allele Identifier: PA280298

Gene: VHL HGNC NCBI

ClinVar Allele:

45566

ClinVar RCV:

RCV000030589

RCV000492408

RCV000533687

ClinVar Variation:

36905

HGVS (amino-acid)	Matching Registered Transcripts
NP_000542.1:p.Tyr175Cys	CA020462 NM_000551.4:c.524A>G