Allele Registry

Canonical Allele Identifier: PA109118

Gene: TMEM216 HGNC NCBI

ClinVar Allele:

214310

ClinVar RCV:

RCV000201742

RCV000595708

RCV001053459

RCV001814113

ClinVar Variation:

217705

HGVS (amino-acid)	Matching Registered Transcripts
NP_001167461.1:p.Arg73Cys	CA277803 NM_001173990.3:c.217C>T