Canonical Allele Identifier: PA2827926842
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 428805
ClinVar RCV Id: RCV000492430
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Trp88_Leu89insArg
CA645369327
NM_001354723.2:c.263_265dup