Allele Registry

Canonical Allele Identifier: PA2827926646

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV003800321

ClinVar Variation:

2943203

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341652.1:p.Pro45Ser	CA351748076 NM_001354723.2:c.133C>T