Allele Registry

Canonical Allele Identifier: PA2827268619

Gene: TIMM50 HGNC NCBI

ClinVar RCV:

RCV002294736

ClinVar Variation:

1712481

HGVS (amino-acid)	Matching Registered Transcripts
NP_001316488.1:p.Arg4Lys	CA405786427 NM_001329559.2:c.11G>A