Canonical Allele Identifier: PA645462558
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 411971
ClinVar RCV Id: RCV000471735 RCV002436462
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Asp9Ala
CA16611161
NM_000551.4:c.26A>C