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