Allele Registry

Canonical Allele Identifier: PA113655

Gene: TIMM8A HGNC NCBI

ClinVar RCV:

RCV000012073

ClinVar Variation:

11321

HGVS (amino-acid)	Matching Registered Transcripts
NP_004076.1:p.Cys66Trp	CA341082 NM_004085.4:c.198C>G