Allele Registry

Canonical Allele Identifier: PA916057034

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV000803524

RCV002381760

RCV003238229

RCV004001665

ClinVar Variation:

648726

HGVS (amino-acid)	Matching Registered Transcripts
NP_937799.1:p.Pro45Leu	CA70042375 NM_198156.3:c.134C>T