Canonical Allele Identifier: PA2828436597
Gene: TMIE HGNC NCBI

Linked Data

ClinVar Variation Id: 3392
ClinVar RCV Id: RCV000003559
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357453.1:p.Arg39Trp
CA252747
NM_001370524.1:c.115C>T