Allele Registry

Canonical Allele Identifier: PA108496

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV000036540

RCV000492137

RCV001379599

ClinVar Variation:

43598

HGVS (amino-acid)	Matching Registered Transcripts
NP_000542.1:p.Glu70Lys	CA020108 NM_000551.4:c.208G>A