Allele Registry

Canonical Allele Identifier: PA100295

Gene: TMEM138 HGNC NCBI

ClinVar Allele:

40147

ClinVar RCV:

RCV000024189

ClinVar Variation:

31190

HGVS (amino-acid)	Matching Registered Transcripts
NP_057548.1:p.Ala126Thr	CA260011 NM_016464.5:c.376G>A