Canonical Allele Identifier: PA108183
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 36900

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Arg107Pro
CA020262
NM_000551.4:c.320G>C
CA645524845
NM_000551.4:c.320_321delinsCA