Canonical Allele Identifier: PA645462771
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 420073
ClinVar RCV Id: RCV000479941 RCV000767237 RCV001201718
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Ile75Ser
CA16617787
NM_000551.4:c.224T>G