Canonical Allele Identifier: PA108163
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 223213
ClinVar RCV Id: RCV000208822 RCV002327073
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Ala149Thr
CA357066
NM_000551.4:c.445G>A