Allele Registry

Canonical Allele Identifier: PA2499303374

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV001300923

RCV002258187

ClinVar Variation:

1004248

HGVS (amino-acid)	Matching Registered Transcripts
NP_937799.1:p.Gly44Asp	CA70042374 NM_198156.3:c.131G>A