Canonical Allele Identifier: PA2827438452
Gene: TRIP12 HGNC NCBI

Linked Data

ClinVar Variation Id: 446138
ClinVar RCV Id: RCV000515140

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001335247.1:p.Arg1623Gln
CA350890921
NM_001348318.2:c.4868G>A