Canonical Allele Identifier: PA2827440448
Gene: TRIP12 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001335255.1:p.Arg379Trp
CA2153351
NM_001348326.2:c.1135C>T