Canonical Allele Identifier: PA2580323012
Gene: TRIM25 HGNC NCBI

Linked Data

ClinVar Variation Id: 2338564
ClinVar RCV Id: RCV004180421

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005073.2:p.Ala594Val
CA399922065
NM_005082.5:c.1781C>T