Allele Registry

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Canonical Allele Identifier: PA916056980

Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 456568

ClinVar RCV Id: RCV000527842

ClinVar Variation Id: 856826

ClinVar RCV Id: RCV001062374 RCV001575478 RCV002379585 RCV004000126 RCV003462593

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_937799.1:p.Ala35_Gly39dup	CA541213520 NM_198156.3:c.99_113dup CA658655747 NM_198156.3:c.103_117dup