Canonical Allele Identifier: PA916056976
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 418538
ClinVar RCV Id: RCV000696976 RCV001294070 RCV001018619 RCV001712442 RCV003900013
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Gly30Glu
CA16617781
NM_198156.3:c.89G>A