Canonical Allele Identifier: PA2827082411
Gene: TRIP11 HGNC NCBI

Linked Data

ClinVar Variation Id: 194742
ClinVar RCV Id: RCV000175183 RCV000841294 RCV001089222 RCV003927601
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308780.1:p.Lys1765Asn
CA201336
NM_001321851.1:c.5295G>T
CA390644795
NM_001321851.1:c.5295G>C