Allele Registry

Canonical Allele Identifier: PA658825846

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV000679034

RCV002458188

ClinVar Variation:

560744

HGVS (amino-acid)	Matching Registered Transcripts
NP_000542.1:p.His115Pro	CA351753626 NM_000551.4:c.344A>C