Allele Registry

Canonical Allele Identifier: PA2827180767

Gene: TMEM183A HGNC NCBI

ClinVar RCV:

RCV004168929

ClinVar Variation:

2323056

HGVS (amino-acid)	Matching Registered Transcripts
NP_001309888.1:p.Ser152Thr	CA344278726 NM_001322959.2:c.454T>A