Canonical Allele Identifier: PA1139734626
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 934978
ClinVar RCV Id: RCV001203476
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Pro185Leu
CA1139655746
NM_001354723.2:c.554C>T