Canonical Allele Identifier: PA645508640
Gene: TMIE HGNC NCBI

Linked Data

ClinVar Variation Id: 287642
ClinVar RCV Id: RCV000336777 RCV000362154
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_671729.2:p.Ser69Phe
CA2357952
NM_147196.3:c.206C>T