Canonical Allele Identifier: PA108450
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 456566
ClinVar RCV Id: RCV000538803 RCV002508221 RCV003302779 RCV003330751
ClinVar Variation Id: 618485
ClinVar RCV Id: RCV000756902 RCV001023281 RCV001382402
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Gln164His
CA351756154
NM_000551.4:c.492G>C
CA351756157
NM_000551.4:c.492G>T