Canonical Allele Identifier: PA2573205669
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1464433
ClinVar RCV Id: RCV001956887
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Phe184Leu
CA2573136139
NM_001354723.2:c.552C>A
CA2592313299
NM_001354723.2:c.552C>G