Canonical Allele Identifier: PA916057192
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_937799.1:p.Gln73Arg
CA351749128
NM_198156.3:c.218A>G