Canonical Allele Identifier: PA2827926747
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 186316
ClinVar RCV Id: RCV000165891 RCV000227354 RCV001545934 RCV003462191
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Glu70Gly
CA020113
NM_001354723.2:c.209A>G