Canonical Allele Identifier: PA2825190901
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1023005
ClinVar RCV Id: RCV001322991
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Arg64Ser
CA351748769
NM_000551.4:c.190C>A