Allele Registry

Canonical Allele Identifier: PA2825190707

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV001300923

RCV002258187

ClinVar Variation:

1004248

HGVS (amino-acid)	Matching Registered Transcripts
NP_000542.1:p.Gly44Asp	CA70042374 NM_000551.4:c.131G>A