Canonical Allele Identifier: PA916057398
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 526674
ClinVar RCV Id: RCV000631270 RCV000997987 RCV002477380 RCV002255483
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Thr100Ala
CA040192
NM_198156.3:c.298A>G