Canonical Allele Identifier: PA916039302
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 816685
ClinVar RCV Id: RCV001007626 RCV001238805 RCV003320779 RCV003325984
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Ser179Pro
CA896160296
NM_001354723.2:c.535T>C