Canonical Allele Identifier: PA108220
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 2216
ClinVar RCV Id: RCV000002300 RCV000325074 RCV000213850 RCV000506694 RCV000627745 RCV003448242
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Arg167Gln
CA020454
NM_000551.4:c.500G>A