Allele Registry

Canonical Allele Identifier: PA2825450168

Gene: TMEM231 HGNC NCBI

ClinVar RCV:

RCV000054806

RCV000162154

RCV001781386

RCV003764728

RCV003915018

RCV003987343

ClinVar Variation:

64619

HGVS (amino-acid)	Matching Registered Transcripts
NP_001070886.1:p.Val222Ile	CA144704 NM_001077418.3:c.664G>A