Canonical Allele Identifier: PA2827440879
Gene: TRIP12 HGNC NCBI

Linked Data

ClinVar Variation Id: 801906
ClinVar RCV Id: RCV000987051

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001335256.1:p.Asp1662Glu
CA350892120
NM_001348327.2:c.4986T>A
CA350892123
NM_001348327.2:c.4986T>G