Allele Registry

Canonical Allele Identifier: PA915963892

Gene: TMEM231 HGNC NCBI

ClinVar Allele:

439090

ClinVar RCV:

RCV000515034

RCV001003228

RCV001865689

RCV003222011

ClinVar Variation:

445818

HGVS (amino-acid)	Matching Registered Transcripts
NP_001070886.1:p.Leu81Phe	CA8176255 NM_001077418.3:c.241C>T