Allele Registry

Canonical Allele Identifier: PA916057310

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV000551615

ClinVar Variation:

456578

HGVS (amino-acid)	Matching Registered Transcripts
NP_937799.1:p.Asn90Thr	CA351750709 NM_198156.3:c.269A>C