Canonical Allele Identifier: PA645463030
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 428803
ClinVar RCV Id: RCV000492569 RCV000590238 RCV002287415 RCV000705307
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Ile151Thr
CA351754359
NM_000551.4:c.452T>C