Canonical Allele Identifier: PA142263
Gene: TMIE HGNC NCBI

Linked Data

ClinVar Variation Id: 47962
ClinVar RCV Id: RCV000041234 RCV000755405 RCV001668170
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_671729.2:p.Lys131del
CA142262
NM_147196.3:c.391_393del