Canonical Allele Identifier: PA2829488431
Gene: TRIP12 HGNC NCBI

Linked Data

ClinVar Variation Id: 446138
ClinVar RCV Id: RCV000515140

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004229.1:p.Arg1595Gln
CA350890921
NM_004238.3:c.4784G>A