Canonical Allele Identifier: PA2827440448
Gene: TRIP12 HGNC NCBI

Linked Data

ClinVar Variation Id: 1305513
ClinVar RCV Id: RCV001768720

Amino-acid Alleles

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