Allele Registry

Canonical Allele Identifier: PA916057279

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV000155449

RCV000413630

RCV000492763

RCV001059327

ClinVar Variation:

178692

HGVS (amino-acid)	Matching Registered Transcripts
NP_937799.1:p.Pro86Ser	CA020180 NM_198156.3:c.256C>T