Allele Registry

Canonical Allele Identifier: PA353852

Gene: VHL HGNC NCBI

ClinVar Allele:

217071

ClinVar RCV:

RCV000203537

RCV001853277

ClinVar Variation:

219158

HGVS (amino-acid)	Matching Registered Transcripts
NP_000542.1:p.Ser183Trp	CA277912 NM_000551.4:c.548C>G