Allele Registry

Canonical Allele Identifier: PA2830430909

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV000002323

RCV001219111

ClinVar Variation:

2235

HGVS (amino-acid)	Matching Registered Transcripts
NP_937799.1:p.His150Asp	CA020495 NM_198156.3:c.448C>G