Allele Registry

Canonical Allele Identifier: PA3057549848

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV005232440

ClinVar Variation:

3765365

HGVS (amino-acid)	Matching Registered Transcripts
NP_937799.1:p.Arg107Cys	CA351751195 NM_198156.3:c.319C>T