Canonical Allele Identifier: PA115420
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 2215

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Ser183Ter
CA645529538
NM_000551.4:c.548_555del