Canonical Allele Identifier: PA2741867958
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 2942719
ClinVar RCV Id: RCV003807885
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Glu130Gln
CA2740090915
NM_001354723.2:c.388G>C