Allele Registry

Canonical Allele Identifier: PA916057249

Gene: VHL HGNC NCBI

ClinVar Allele:

45560

ClinVar RCV:

RCV000030582

RCV000129974

RCV001034657

RCV001547784

RCV003460493

ClinVar Variation:

36899

HGVS (amino-acid)	Matching Registered Transcripts
NP_937799.1:p.Pro81Leu	CA020154 NM_198156.3:c.242C>T