Canonical Allele Identifier: PA2827926931
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 2583006
ClinVar RCV Id: RCV003334249
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Ile109Val
CA351751254
NM_001354723.2:c.325A>G