Allele Registry

Canonical Allele Identifier: PA916027890

Gene: TMEM138 HGNC NCBI

ClinVar Allele:

40147

ClinVar RCV:

RCV000024189

ClinVar Variation:

31190

HGVS (amino-acid)	Matching Registered Transcripts
NP_001317210.1:p.Ala68Thr	CA260011 NM_001330281.2:c.202G>A