Canonical Allele Identifier: PA2830430557
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1712100
ClinVar RCV Id: RCV002293818 RCV004047631
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Val114Ala
CA351756034
NM_198156.3:c.341T>C