Allele Registry

Canonical Allele Identifier: PA645382171

Gene: TMEM216 HGNC NCBI

ClinVar RCV:

RCV000291175

RCV000345935

RCV000401686

RCV001240998

RCV001788191

ClinVar Variation:

289981

HGVS (amino-acid)	Matching Registered Transcripts
NP_001167462.1:p.Val47Ala	CA6034711 NM_001173991.3:c.140T>C