Allele Registry

Canonical Allele Identifier: PA2826865737

Gene: TRIM69 HGNC NCBI

ClinVar RCV:

RCV001779427

ClinVar Variation:

1321332

HGVS (amino-acid)	Matching Registered Transcripts
NP_001288075.1:p.Phe231Leu	CA7536708 NM_001301146.2:c.693C>A CA392299376 NM_001301146.2:c.691T>C CA392299381 NM_001301146.2:c.693C>G