Canonical Allele Identifier: PA2573205646
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1442546
ClinVar RCV Id: RCV001953057

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Gly153_Arg154del
CA896160270
NM_001354723.2:c.458_463del