Canonical Allele Identifier: PA2827926942
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 223187
ClinVar RCV Id: RCV000208866 RCV000492675 RCV001204150
ClinVar Variation Id: 2673948
ClinVar RCV Id: RCV003450556
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Ser111Arg
CA040305
NM_001354723.2:c.333C>G
CA351751320
NM_001354723.2:c.331A>C
CA351751338
NM_001354723.2:c.333C>A