Canonical Allele Identifier: PA196920
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 135955
ClinVar RCV Id: RCV000123106 RCV000166872 RCV003997420
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Glu94Lys
CA020237
NM_000551.4:c.280G>A