Allele Registry

Canonical Allele Identifier: PA2580359637

Gene: TIMM22 HGNC NCBI

ClinVar Allele:

2313789

ClinVar RCV:

RCV004164121

ClinVar Variation:

2319702

HGVS (amino-acid)	Matching Registered Transcripts
NP_037469.2:p.Ser145Ala	CA8264466 NM_013337.4:c.433T>G