Canonical Allele Identifier: PA2827926922
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 36900
ClinVar RCV Id: RCV000030583 RCV000486047 RCV000492682 RCV000816283
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Arg107Pro
CA020262
NM_001354723.2:c.320G>C
CA645524845
NM_001354723.2:c.320_321delinsCA