Canonical Allele Identifier: PA2827081796
Gene: TRIP11 HGNC NCBI

Linked Data

ClinVar Variation Id: 314970
ClinVar RCV Id: RCV000406125 RCV000593586 RCV002278417
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308780.1:p.Leu426Ser
CA7313969
NM_001321851.1:c.1277T>C