Canonical Allele Identifier: PA108549
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 223175
ClinVar RCV Id: RCV000208845

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Gly93Cys
CA357106
NM_000551.4:c.277G>T