Canonical Allele Identifier: PA1139734423
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 836703
ClinVar RCV Id: RCV001037891
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Arg160Cys
CA896160284
NM_001354723.2:c.478C>T