Canonical Allele Identifier: PA108613
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 161401
ClinVar RCV Id: RCV000148921 RCV000524495 RCV000480432 RCV000569566 RCV002467588 RCV003387773
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Ile180Val
CA020469
NM_000551.4:c.538A>G