Canonical Allele Identifier: PA2499252061
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1051126
ClinVar RCV Id: RCV001359121
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Ser190Thr
CA1345067569
NM_001354723.2:c.569G>C