Allele Registry

Canonical Allele Identifier: PA916057315

Gene: VHL HGNC NCBI

ClinVar Allele:

224903

ClinVar RCV:

RCV000208809

RCV002426982

ClinVar Variation:

223172

HGVS (amino-acid)	Matching Registered Transcripts
NP_937799.1:p.Asn90Ile	CA357043 NM_198156.3:c.269A>T