Canonical Allele Identifier: PA2827926758
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 584568
ClinVar RCV Id: RCV000708763 RCV001059124 RCV002469274 RCV003460991 RCV003403638
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Gln73Arg
CA351749128
NM_001354723.2:c.218A>G