Canonical Allele Identifier: PA2829488142
Gene: TRIP12 HGNC NCBI

Linked Data

ClinVar Variation Id: 1379554
ClinVar RCV Id: RCV001883831

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004229.1:p.Ala220Val
CA350895615
NM_004238.3:c.659C>T