Allele Registry

Canonical Allele Identifier: PA2827926638

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV001300923

RCV002258187

ClinVar Variation:

1004248

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341652.1:p.Gly44Asp	CA70042374 NM_001354723.2:c.131G>A