Canonical Allele Identifier: PA916057127
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 581453
ClinVar RCV Id: RCV000705281
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Pro61Arg
CA351748722
NM_198156.3:c.182C>G