Canonical Allele Identifier: PA645462544
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 411975
ClinVar RCV Id: RCV000456617 RCV002436463 RCV003441887 RCV004001988
ClinVar Variation Id: 846969
ClinVar RCV Id: RCV001050407
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Asp9Glu
CA16611250
NM_000551.4:c.27C>A
CA351747082
NM_000551.4:c.27C>G