Canonical Allele Identifier: PA357021
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 223185
ClinVar RCV Id: RCV000208794
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Ser111Ile
CA357019
NM_000551.4:c.332G>T