Allele Registry

Canonical Allele Identifier: PA2827926828

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV000155449

RCV000413630

RCV000492763

RCV001059327

ClinVar Variation:

178692

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341652.1:p.Pro86Ser	CA020180 NM_001354723.2:c.256C>T