Allele Registry

Canonical Allele Identifier: PA2826865687

Gene: TRIM69 HGNC NCBI

ClinVar RCV:

RCV001779427

ClinVar Variation:

1321332

HGVS (amino-acid)	Matching Registered Transcripts
NP_001288074.1:p.Phe247Leu	CA7536708 NM_001301145.2:c.741C>A CA392299376 NM_001301145.2:c.739T>C CA392299381 NM_001301145.2:c.741C>G