Canonical Allele Identifier: PA916057397
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 644033
ClinVar RCV Id: RCV000797870 RCV002255525
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Thr100Met
CA351750989
NM_198156.3:c.299C>T