Allele Registry

Canonical Allele Identifier: PA2825450002

Gene: TMEM231 HGNC NCBI

ClinVar Allele:

268656

ClinVar RCV:

RCV000443211

RCV001087198

ClinVar Variation:

284419

HGVS (amino-acid)	Matching Registered Transcripts
NP_001070886.1:p.Ala31Thr	CA8176305 NM_001077418.3:c.91G>A