Allele Registry

Canonical Allele Identifier: PA645463298

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV000492180

RCV000547627

ClinVar Variation:

428810

HGVS (amino-acid)	Matching Registered Transcripts
NP_000542.1:p.Val194Gly	CA351756475 NM_000551.4:c.581T>G