Canonical Allele Identifier: PA658667199
Gene: TRIP11 HGNC NCBI

Linked Data

ClinVar Variation Id: 449194
ClinVar RCV Id: RCV001087540 RCV002279309 RCV000729388 RCV003915465
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004230.2:p.Pro1877Thr
CA7313094
NM_004239.4:c.5629C>A