Allele Registry

Canonical Allele Identifier: PA108696

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV000161088

RCV000208846

RCV000492547

RCV001072084

ClinVar Variation:

182980

HGVS (amino-acid)	Matching Registered Transcripts
NP_000542.1:p.Leu158Pro	CA020399 NM_000551.4:c.473T>C CA645525048 NM_000551.4:c.473_474delinsCC