Canonical Allele Identifier: PA2580556365
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 2474533
ClinVar RCV Id: RCV003203225

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Glu53del
CA2580614138
NM_198156.3:c.157_159del