Canonical Allele Identifier: PA2827926835
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 456577
ClinVar RCV Id: RCV000587190 RCV000679026 RCV000558602 RCV002431533 RCV003459186
ClinVar Variation Id: 496053
ClinVar RCV Id: RCV000589476 RCV000631292
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Trp88Arg
CA351750667
NM_001354723.2:c.262T>C
CA351750671
NM_001354723.2:c.262T>A