Allele Registry

Canonical Allele Identifier: PA645422518

Gene: TMEM216 HGNC NCBI

ClinVar RCV:

RCV000273916

RCV000368499

RCV000734945

RCV001093978

RCV002520731

ClinVar Variation:

305080

HGVS (amino-acid)	Matching Registered Transcripts
NP_057583.2:p.Met59Val	CA6034753 NM_016499.6:c.175A>G