Allele Registry

Canonical Allele Identifier: PA2830430907

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV003794414

ClinVar Variation:

2937784

HGVS (amino-acid)	Matching Registered Transcripts
NP_937799.1:p.His150Tyr	CA351756416 NM_198156.3:c.448C>T