Allele Registry

Canonical Allele Identifier: PA108969

Gene: VHL HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000002321

RCV000115744

RCV000213077

RCV000418681

RCV000656990

RCV001080004

RCV001843451

RCV002467489

RCV003225718

ClinVar Variation:

2233

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000542.1:p.Pro81Ser	CA020148 NM_000551.4:c.241C>T