Allele Registry

Canonical Allele Identifier: PA658669183

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV000551615

ClinVar Variation:

456578

HGVS (amino-acid)	Matching Registered Transcripts
NP_000542.1:p.Asn90Thr	CA351750709 NM_000551.4:c.269A>C