Allele Registry

Canonical Allele Identifier: PA1139764408

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV001051596

ClinVar Variation:

847948

HGVS (amino-acid)	Matching Registered Transcripts
NP_937799.1:p.Glu70Gln	CA351748955 NM_198156.3:c.208G>C