Canonical Allele Identifier: PA2580228813
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 2119234
ClinVar RCV Id: RCV003054555

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Gly175Asp
CA1345067491
NM_001354723.2:c.524G>A