Allele Registry

Canonical Allele Identifier: PA2827926845

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV000551615

ClinVar Variation:

456578

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341652.1:p.Asn90Thr	CA351750709 NM_001354723.2:c.269A>C