Allele Registry

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Canonical Allele Identifier: PA2827926475

Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 411975

ClinVar RCV Id: RCV000456617 RCV002436463 RCV003441887 RCV004001988

ClinVar Variation Id: 846969

ClinVar RCV Id: RCV001050407

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341652.1:p.Asp9Glu	CA16611250 NM_001354723.2:c.27C>A CA351747082 NM_001354723.2:c.27C>G