Canonical Allele Identifier: PA2825190658
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1437880

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Gly39Val
CA70042314
NM_000551.4:c.116G>T