Allele Registry

Canonical Allele Identifier: PA916057032

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV000800391

ClinVar Variation:

646162

HGVS (amino-acid)	Matching Registered Transcripts
NP_937799.1:p.Gly44Ser	CA351748044 NM_198156.3:c.130G>A