Canonical Allele Identifier: PA2827442468
Gene: TRIP12 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001335263.1:p.Arg350Trp
CA2153351
NM_001348334.1:c.1048C>T