Allele Registry

Canonical Allele Identifier: PA2827293353

Gene: TMEM138 HGNC NCBI

ClinVar RCV:

RCV000024187

RCV000423402

ClinVar Variation:

31188

HGVS (amino-acid)	Matching Registered Transcripts
NP_001317210.1:p.His38Arg	CA260009 NM_001330281.2:c.113A>G