Canonical Allele Identifier: PA1139691523
Gene: TMEM216 HGNC NCBI

Linked Data

ClinVar Variation Id: 855127
ClinVar RCV Id: RCV001060316 RCV001275257 RCV003160483
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001167462.1:p.Arg4Gln
CA222894436
NM_001173991.3:c.11G>A