Allele Registry

Canonical Allele Identifier: PA2825190702

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV001338248

RCV003313216

ClinVar Variation:

1035388

HGVS (amino-acid)	Matching Registered Transcripts
NP_000542.1:p.Ser43Pro	CA351748001 NM_000551.4:c.127T>C