Canonical Allele Identifier: PA2580117476
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1733659
ClinVar RCV Id: RCV003094283 RCV002452533
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Ala122Glu
CA351753772
NM_000551.4:c.365C>A