Allele Registry

Canonical Allele Identifier: PA916056879

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV000456617

RCV001050407

RCV002436463

RCV003441887

RCV004001988

ClinVar Variation:

411975

846969

HGVS (amino-acid)	Matching Registered Transcripts
NP_937799.1:p.Asp9Glu	CA16611250 NM_198156.3:c.27C>A CA351747082 NM_198156.3:c.27C>G