Canonical Allele Identifier: PA2741958608
Gene: TMEM216 HGNC NCBI

Linked Data

ClinVar Variation Id: 2714687
ClinVar RCV Id: RCV003496488

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057583.2:p.Gly7Val
CA380685151
NM_016499.6:c.20G>T