Allele Registry

Canonical Allele Identifier: PA2830430797

Gene: VHL HGNC NCBI

ClinVar Allele:

45566

ClinVar RCV:

RCV000030589

RCV000492408

RCV000533687

ClinVar Variation:

36905

HGVS (amino-acid)	Matching Registered Transcripts
NP_937799.1:p.Tyr134Cys	CA020462 NM_198156.3:c.401A>G