Canonical Allele Identifier: PA916056851
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 238114
ClinVar RCV Id: RCV000226904 RCV002418000 RCV003226914
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Arg3Trp
CA10582110
NM_198156.3:c.7C>T