Canonical Allele Identifier: PA2825190583
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 2184560
ClinVar RCV Id: RCV002603364
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Glu26Gly
CA351747453
NM_000551.4:c.77A>G