Canonical Allele Identifier: PA2828436606
Gene: TMIE HGNC NCBI

Linked Data

ClinVar Variation Id: 262622
ClinVar RCV Id: RCV000253873 RCV001552669
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357453.1:p.Lys77_Lys78del
CA142260
NM_001370524.1:c.229_232delinsG
CA2358019
NM_001370524.1:c.229_234del