Canonical Allele Identifier: PA916057385
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 2223
ClinVar RCV Id: RCV000002309 RCV000492094 RCV000679029 RCV000684783 RCV003891425
ClinVar Variation Id: 2940951
ClinVar RCV Id: RCV003792213
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Tyr98His
CA020246
NM_198156.3:c.292T>C
CA2740090907
NM_198156.3:c.291_292delinsAC