Canonical Allele Identifier: PA109148
Gene: TMEM216 HGNC NCBI

Linked Data

ClinVar Variation Id: 200
ClinVar RCV Id: RCV000000223

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001167461.1:p.Gly77Ala
CA114039
NM_001173990.3:c.230G>C