Canonical Allele Identifier: PA2826096332
Gene: TMEM216 HGNC NCBI

Linked Data

ClinVar Variation Id: 2047538
ClinVar RCV Id: RCV002904380
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001167461.1:p.Phe76Ile
CA380685194
NM_001173990.3:c.226T>A