Canonical Allele Identifier: PA2827926789
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 93326
ClinVar RCV Id: RCV000079207 RCV000254892 RCV000492165 RCV001034687
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Asn78Ser
CA020131
NM_001354723.2:c.233A>G