Canonical Allele Identifier: PA2827926836
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 223171
ClinVar RCV Id: RCV000208827 RCV000492552 RCV000537014
ClinVar Variation Id: 580847
ClinVar RCV Id: RCV000704506
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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