Allele Registry

Canonical Allele Identifier: PA2827926627

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV003187669

ClinVar Variation:

2451973

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341652.1:p.Glu42Asp	CA351747990 NM_001354723.2:c.126G>C CA351747994 NM_001354723.2:c.126G>T