Canonical Allele Identifier: PA2827441229
Gene: TRIP12 HGNC NCBI

Linked Data

ClinVar Variation Id: 1379554
ClinVar RCV Id: RCV001883831
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001335258.1:p.Ala262Val
CA350895615
NM_001348329.2:c.785C>T