Canonical Allele Identifier: PA201337
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_004230.2:p.Lys1766Asn
CA201336
NM_004239.4:c.5298G>T
CA390644795
NM_004239.4:c.5298G>C