Allele Registry

Canonical Allele Identifier: PA2827180707

Gene: TMEM183A HGNC NCBI

ClinVar RCV:

RCV004168929

ClinVar Variation:

2323056

HGVS (amino-acid)	Matching Registered Transcripts
NP_001309885.1:p.Ser182Thr	CA344278726 NM_001322956.2:c.544T>A