Canonical Allele Identifier: PA2827082500
Gene: TRIP11 HGNC NCBI

Linked Data

ClinVar Variation Id: 426917
ClinVar RCV Id: RCV000488927 RCV002063835 RCV004023259
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308780.1:p.Ala1962Thr
CA7313033
NM_001321851.1:c.5884G>A