Canonical Allele Identifier: PA1139691532
Gene: TMEM216 HGNC NCBI

Linked Data

ClinVar Variation Id: 857506

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001167462.1:p.Arg14Trp
CA6034697
NM_001173991.3:c.40C>T