Canonical Allele Identifier: PA2827081913
Gene: TRIP11 HGNC NCBI

Linked Data

ClinVar Variation Id: 314961
ClinVar RCV Id: RCV000380572
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308780.1:p.Asp785Ala
CA7313789
NM_001321851.1:c.2354A>C