Canonical Allele Identifier: PA1139764419
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 859253
ClinVar RCV Id: RCV001065319
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Gln73Leu
CA351749113
NM_198156.3:c.218A>T