Canonical Allele Identifier: PA2499233374
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1018515
ClinVar RCV Id: RCV001317824
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Ala149Val
CA351754317
NM_000551.4:c.446C>T