Canonical Allele Identifier: PA2829840702
Gene: TMEM216 HGNC NCBI

Linked Data

ClinVar Variation Id: 1433371
ClinVar RCV Id: RCV001960088
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057583.2:p.Phe14Cys
CA380685191
NM_016499.6:c.41T>G