Allele Registry

Canonical Allele Identifier: PA109023

Gene: VHL HGNC NCBI

ClinVar Variation Id: 223187

ClinVar Variation Id: 2673948

ClinVar RCV Id: RCV003450556

HGVS (amino-acid)	Matching Registered Transcripts
NP_000542.1:p.Ser111Arg	CA040305 NM_000551.4:c.333C>G CA351751320 NM_000551.4:c.331A>C CA351751338 NM_000551.4:c.333C>A