Canonical Allele Identifier: PA142261
Gene: TMIE HGNC NCBI

Linked Data

ClinVar Variation Id: 47961
ClinVar RCV Id: RCV000041233
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_671729.2:p.Lys130_Lys131delinsGlu
CA142260
NM_147196.3:c.388_391delinsG