Allele Registry

Canonical Allele Identifier: PA2580540659

Gene: TRIM69 HGNC NCBI

ClinVar RCV:

RCV004072299

ClinVar Variation:

2203956

HGVS (amino-acid)	Matching Registered Transcripts
NP_892030.3:p.Lys138Gln	CA7536445 NM_182985.5:c.412A>C