Canonical Allele Identifier: PA2827926906
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 645405
ClinVar RCV Id: RCV000799472 RCV003322824 RCV004001627
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Pro102Leu
CA351751047
NM_001354723.2:c.305C>T