Canonical Allele Identifier: PA2829488428
Gene: TRIP12 HGNC NCBI

Linked Data

ClinVar Variation Id: 801906
ClinVar RCV Id: RCV000987051

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004229.1:p.Asp1587Glu
CA350892120
NM_004238.3:c.4761T>A
CA350892123
NM_004238.3:c.4761T>G