Allele Registry

Canonical Allele Identifier: PA2573100804

Gene: TRIM69 HGNC NCBI

ClinVar RCV:

RCV001779427

ClinVar Variation:

1321332

HGVS (amino-acid)	Matching Registered Transcripts
NP_892030.3:p.Phe468Leu	CA7536708 NM_182985.5:c.1404C>A CA392299376 NM_182985.5:c.1402T>C CA392299381 NM_182985.5:c.1404C>G