Canonical Allele Identifier: PA916056844
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 411967
ClinVar RCV Id: RCV000458939 RCV000579235 RCV000663055 RCV002418424
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Met1Leu