Allele Registry

Canonical Allele Identifier: PA108567

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV000822511

RCV003169035

ClinVar Variation:

664415

HGVS (amino-acid)	Matching Registered Transcripts
NP_000542.1:p.His115Arg	CA70049376 NM_000551.4:c.344A>G