Canonical Allele Identifier: PA339802
Gene: TMEM216 HGNC NCBI

Linked Data

ClinVar Variation Id: 197
ClinVar RCV Id: RCV000000220 RCV000255378 RCV000409114 RCV000465185 RCV000624413 RCV000779066 RCV001787358
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001167462.1:p.Arg73Leu
CA339800
NM_001173991.3:c.218G>T