Allele Registry

Canonical Allele Identifier: PA2499303373

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV001338248

RCV003313216

ClinVar Variation:

1035388

HGVS (amino-acid)	Matching Registered Transcripts
NP_937799.1:p.Ser43Pro	CA351748001 NM_198156.3:c.127T>C