Allele Registry

Canonical Allele Identifier: PA109213

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV000036543

RCV000487045

RCV000492752

RCV000631280

ClinVar Variation:

43600

HGVS (amino-acid)	Matching Registered Transcripts
NP_000542.1:p.Tyr156Cys	CA020394 NM_000551.4:c.467A>G