Canonical Allele Identifier: PA913197417
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 633017
ClinVar RCV Id: RCV000780789
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Asn90Tyr
CA351750702
NM_000551.4:c.268A>T