Canonical Allele Identifier: PA2830430912
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 825946
ClinVar RCV Id: RCV001024492 RCV001294333
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Pro151Arg
CA70052552
NM_198156.3:c.452C>G