Canonical Allele Identifier: PA2826096538
Gene: TMEM216 HGNC NCBI

Linked Data

ClinVar Variation Id: 2714687
ClinVar RCV Id: RCV003496488
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001167462.1:p.Gly68Val
CA380685151
NM_001173991.3:c.203G>T