Canonical Allele Identifier: PA916056961
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 93330
ClinVar RCV Id: RCV000079211 RCV000126300 RCV000119213 RCV000224298 RCV001082579 RCV002467563
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Pro25Leu
CA020538
NM_198156.3:c.74C>T