Canonical Allele Identifier: PA2827926836
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 223171
ClinVar Variation Id: 580847
ClinVar RCV Id: RCV000704506

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Trp88Cys
CA357078
NM_001354723.2:c.264G>T
CA351750678
NM_001354723.2:c.264G>C