Canonical Allele Identifier: PA109152
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
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Trp88Arg
CA351750667
NM_000551.4:c.262T>C
CA351750671
NM_000551.4:c.262T>A