Canonical Allele Identifier: PA658719948
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 496063
ClinVar RCV Id: RCV000589183 RCV002377215
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Gln132Pro
CA351753958
NM_000551.4:c.395A>C