Canonical Allele Identifier: PA2827293478
Gene: TMEM216 HGNC NCBI

Linked Data

ClinVar Variation Id: 198
ClinVar RCV Id: RCV000000221 RCV000024013 RCV001038780
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317214.1:p.Arg12His
CA129626
NM_001330285.2:c.35G>A