Allele Registry

Canonical Allele Identifier: PA108715

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV000002319

RCV001231697

RCV003298026

RCV004018540

ClinVar Variation:

2231

HGVS (amino-acid)	Matching Registered Transcripts
NP_000542.1:p.Leu163Pro	CA020423 NM_000551.4:c.488T>C CA645525064 NM_000551.4:c.488_489delinsCT