Allele Registry

Canonical Allele Identifier: PA109232

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV000002309

RCV000492094

RCV000679029

RCV000684783

RCV003792213

RCV003891425

ClinVar Variation:

2223

2940951

HGVS (amino-acid)	Matching Registered Transcripts
NP_000542.1:p.Tyr98His	CA020246 NM_000551.4:c.292T>C CA2740090907 NM_000551.4:c.291_292delinsAC