Allele Registry

Canonical Allele Identifier: PA109135

Gene: TMEM216 HGNC NCBI

ClinVar RCV:

RCV000000220

RCV000255378

RCV000409114

RCV000465185

RCV000624413

RCV000779066

RCV001787358

ClinVar Variation:

197

HGVS (amino-acid)	Matching Registered Transcripts
NP_001167461.1:p.Arg73Leu	CA339800 NM_001173990.3:c.218G>T