Canonical Allele Identifier: PA2573205625
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1376202
ClinVar RCV Id: RCV001871216
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Glu130Lys
CA2573136099
NM_001354723.2:c.388G>A