Canonical Allele Identifier: PA2573170878
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1518457
ClinVar RCV Id: RCV002021758 RCV002486749 RCV004011159
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Arg177Thr
CA351756242
NM_000551.4:c.530G>C