Allele Registry

Canonical Allele Identifier: PA2830430562

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV000208862

RCV001289415

ClinVar Variation:

223223

HGVS (amino-acid)	Matching Registered Transcripts
NP_937799.1:p.Thr116Ile	CA357133 NM_198156.3:c.347C>T