Canonical Allele Identifier: PA109122
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 496055
ClinVar RCV Id: RCV000589007
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Thr105Pro
CA351751116
NM_000551.4:c.313A>C