Allele Registry

Canonical Allele Identifier: PA916057188

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV000686913

RCV002424590

ClinVar Variation:

566960

HGVS (amino-acid)	Matching Registered Transcripts
NP_937799.1:p.Gln73Glu	CA70042515 NM_198156.3:c.217C>G