Allele Registry

Canonical Allele Identifier: PA109015

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV000155449

RCV000413630

RCV000492763

RCV001059327

ClinVar Variation:

178692

HGVS (amino-acid)	Matching Registered Transcripts
NP_000542.1:p.Pro86Ser	CA020180 NM_000551.4:c.256C>T