Allele Registry

Canonical Allele Identifier: PA2573170890

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV001988653

RCV003464363

ClinVar Variation:

1488572

HGVS (amino-acid)	Matching Registered Transcripts
NP_000542.1:p.Pro192Thr	CA351756433 NM_000551.4:c.574C>A