Allele Registry

Canonical Allele Identifier: PA916057448

Gene: VHL HGNC NCBI

ClinVar Variation Id: 223187

ClinVar Variation Id: 2673948

ClinVar RCV Id: RCV003450556

HGVS (amino-acid)	Matching Registered Transcripts
NP_937799.1:p.Ser111Arg	CA040305 NM_198156.3:c.333C>G CA351751320 NM_198156.3:c.331A>C CA351751338 NM_198156.3:c.333C>A