Canonical Allele Identifier: PA108847
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 825149
ClinVar RCV Id: RCV001023000
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Lys159Glu
CA351756078
NM_000551.4:c.475A>G