Allele Registry

Canonical Allele Identifier: PA2826865645

Gene: TRIM69 HGNC NCBI

ClinVar RCV:

RCV001779427

ClinVar Variation:

1321332

HGVS (amino-acid)	Matching Registered Transcripts
NP_001288073.1:p.Phe264Leu	CA7536708 NM_001301144.2:c.792C>A CA392299376 NM_001301144.2:c.790T>C CA392299381 NM_001301144.2:c.792C>G