Allele Registry

Canonical Allele Identifier: PA2580540654

Gene: TRIM69 HGNC NCBI

ClinVar RCV:

RCV004079023

ClinVar Variation:

2208605

HGVS (amino-acid)	Matching Registered Transcripts
NP_892030.3:p.Leu124Arg	CA7536434 NM_182985.5:c.371T>G