Canonical Allele Identifier: PA357137
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 223184
ClinVar RCV Id: RCV000208864 RCV000492448 RCV001379601 RCV003897458
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Arg107His
CA357135
NM_000551.4:c.320G>A