Canonical Allele Identifier: PA108327
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 625225
ClinVar RCV Id: RCV000767240
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Asn78His
CA351749283
NM_000551.4:c.232A>C