Canonical Allele Identifier: PA2827926610
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 456570

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Gly39Asp
CA351747884
NM_001354723.2:c.116G>A