Allele Registry

Canonical Allele Identifier: PA2573170875

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV002016917

ClinVar Variation:

1511818

HGVS (amino-acid)	Matching Registered Transcripts
NP_000542.1:p.Val166Ile	CA351756173 NM_000551.4:c.496G>A