Canonical Allele Identifier: PA117562
Gene: TRIP11 HGNC NCBI

Linked Data

ClinVar Variation Id: 692167
ClinVar RCV Id: RCV000853513 RCV003489941
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004230.2:p.Trp1224Ter