Allele Registry

Canonical Allele Identifier: PA3057538461

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV000813757

RCV002440776

RCV003461218

RCV005029498

ClinVar Variation:

657192

HGVS (amino-acid)	Matching Registered Transcripts
NP_937799.1:p.Ser38_Glu52dup	CA915941834 NM_198156.3:c.112_156dup