Canonical Allele Identifier: PA2827438260
Gene: TRIP12 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001335247.1:p.Ala220Val
CA350895615
NM_001348318.2:c.659C>T