Canonical Allele Identifier: PA108240
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 2218

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Arg167Trp
CA020450
NM_000551.4:c.499C>T