Allele Registry

Canonical Allele Identifier: PA2825190703

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV002269204

ClinVar Variation:

1697920

HGVS (amino-acid)	Matching Registered Transcripts
NP_000542.1:p.Ser43Tyr	CA70042349 NM_000551.4:c.128C>A