Canonical Allele Identifier: PA238699
Gene: TMEM216 HGNC NCBI

Linked Data

ClinVar Variation Id: 193189
ClinVar RCV Id: RCV000173235 RCV000345023 RCV000391281 RCV001094053 RCV004535185
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001167461.1:p.Leu2Pro
CA238698
NM_001173990.3:c.5T>C