Allele Registry

Canonical Allele Identifier: PA2827926632

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV001338248

RCV003313216

ClinVar Variation:

1035388

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341652.1:p.Ser43Pro	CA351748001 NM_001354723.2:c.127T>C