Canonical Allele Identifier: PA108856
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 496059
ClinVar RCV Id: RCV000588483 RCV000631289 RCV002456285
ClinVar Variation Id: 625240
ClinVar RCV Id: RCV000767262 RCV002458373 RCV000821822
ClinVar Variation Id: 1732864
ClinVar RCV Id: RCV002455064
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Phe119Leu
CA351753707
NM_000551.4:c.355T>C
CA351753724
NM_000551.4:c.357C>A
CA351753726
NM_000551.4:c.357C>G