Allele Registry

Canonical Allele Identifier: PA2826096656

Gene: TMEM216 HGNC NCBI

ClinVar RCV:

RCV000273916

RCV000368499

RCV000734945

RCV001093978

RCV002520731

ClinVar Variation:

305080

HGVS (amino-acid)	Matching Registered Transcripts
NP_001167462.1:p.Met120Val	CA6034753 NM_001173991.3:c.358A>G