Allele Registry

Canonical Allele Identifier: PA2827926641

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV001882271

RCV004041460

ClinVar Variation:

1392798

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341652.1:p.Gly44Val	CA351748065 NM_001354723.2:c.131G>T