Canonical Allele Identifier: PA916057456
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 223189
ClinVar RCV Id: RCV000208852 RCV000219736 RCV000631262 RCV001289414
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Tyr112Cys
CA357115
NM_198156.3:c.335A>G