Canonical Allele Identifier: PA2827926522
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 486722
ClinVar RCV Id: RCV000563088
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Ala18Ser
CA351747273
NM_001354723.2:c.52G>T