Canonical Allele Identifier: PA129627
Gene: TMEM216 HGNC NCBI

Linked Data

ClinVar Variation Id: 198
ClinVar RCV Id: RCV000000221 RCV000024013 RCV001038780
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057583.2:p.Arg12His
CA129626
NM_016499.6:c.35G>A