Allele Registry

Canonical Allele Identifier: PA2830161831

Gene: TRIM69 HGNC NCBI

ClinVar RCV:

RCV001779427

ClinVar Variation:

1321332

HGVS (amino-acid)	Matching Registered Transcripts
NP_542783.2:p.Phe309Leu	CA7536708 NM_080745.5:c.927C>A CA392299376 NM_080745.5:c.925T>C CA392299381 NM_080745.5:c.927C>G