Allele Registry

Canonical Allele Identifier: PA2825190953

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV001051596

ClinVar Variation:

847948

HGVS (amino-acid)	Matching Registered Transcripts
NP_000542.1:p.Glu70Gln	CA351748955 NM_000551.4:c.208G>C