Canonical Allele Identifier: PA916057112
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 644898
ClinVar RCV Id: RCV000798890 RCV001012789 RCV003467375
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Gly57Trp
CA351748610
NM_198156.3:c.169G>T