Allele Registry

Canonical Allele Identifier: PA108356

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV000208830

RCV000679035

RCV000801501

RCV004020567

ClinVar Variation:

223200

HGVS (amino-acid)	Matching Registered Transcripts
NP_000542.1:p.Asp121Gly	CA357083 NM_000551.4:c.362A>G