Allele Registry

Canonical Allele Identifier: PA100324

Gene: TMEM138 HGNC NCBI

ClinVar Allele:

40148

ClinVar RCV:

RCV000024190

ClinVar Variation:

31191

HGVS (amino-acid)	Matching Registered Transcripts
NP_057548.1:p.Tyr130Cys	CA260012 NM_016464.5:c.389A>G