Canonical Allele Identifier: PA2826096310
Gene: TMEM216 HGNC NCBI

Linked Data

ClinVar Variation Id: 2714687
ClinVar RCV Id: RCV003496488

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001167461.1:p.Gly68Val
CA380685151
NM_001173990.3:c.203G>T