Canonical Allele Identifier: PA2827926914
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 223183
ClinVar RCV Id: RCV000208803 RCV000679030
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Gly104Val
CA357033
NM_001354723.2:c.311G>T