Allele Registry

Canonical Allele Identifier: PA913197544

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV000767279

ClinVar Variation:

625253

HGVS (amino-acid)	Matching Registered Transcripts
NP_000542.1:p.Gln164Glu	CA351756145 NM_000551.4:c.490C>G