Canonical Allele Identifier: PA645463121
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 428799
ClinVar RCV Id: RCV000492510 RCV000767282
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Arg167Pro
CA351756177
NM_000551.4:c.500G>C