Allele Registry

Canonical Allele Identifier: PA100308

Gene: TMEM138 HGNC NCBI

ClinVar RCV:

RCV000024188

ClinVar Variation:

31189

HGVS (amino-acid)	Matching Registered Transcripts
NP_057548.1:p.Ala127Val	CA260010 NM_016464.5:c.380C>T