Allele Registry

Canonical Allele Identifier: PA2741815443

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV003794414

ClinVar Variation:

2937784

HGVS (amino-acid)	Matching Registered Transcripts
NP_000542.1:p.His191Tyr	CA351756416 NM_000551.4:c.571C>T