Allele Registry

Canonical Allele Identifier: PA109132

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV000208862

RCV001289415

ClinVar Variation:

223223

HGVS (amino-acid)	Matching Registered Transcripts
NP_000542.1:p.Thr157Ile	CA357133 NM_000551.4:c.470C>T