Allele Registry

Canonical Allele Identifier: PA2499233386

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV001316784

ClinVar Variation:

1017610

HGVS (amino-acid)	Matching Registered Transcripts
NP_000542.1:p.Glu186Gln	CA351756383 NM_000551.4:c.556G>C