Canonical Allele Identifier: PA2825190448
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1499649
ClinVar RCV Id: RCV002042393 RCV003230725
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Trp8Gly
CA351747059
NM_000551.4:c.22T>G