Allele Registry

Canonical Allele Identifier: PA108400

Gene: VHL HGNC NCBI

ClinVar Allele:

52773

3113298

ClinVar RCV:

RCV000036548

RCV002513389

RCV003812589

ClinVar Variation:

43604

2951902

HGVS (amino-acid)	Matching Registered Transcripts
NP_000542.1:p.Cys162Phe	CA020418 NM_000551.4:c.485G>T CA2740090901 NM_000551.4:c.485_486delinsTT