Canonical Allele Identifier: PA277804
Gene: TMEM216 HGNC NCBI

Linked Data

ClinVar Variation Id: 217705
ClinVar RCV Id: RCV000201742 RCV000595708 RCV001053459 RCV001814113
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057583.2:p.Arg12Cys
CA277803
NM_016499.6:c.34C>T