Allele Registry

Canonical Allele Identifier: PA261935

Gene: TMIE HGNC NCBI

ClinVar RCV:

RCV000041230

ClinVar Variation:

47958

HGVS (amino-acid)	Matching Registered Transcripts
NP_671729.2:p.Arg84Leu	CA261934 NM_147196.3:c.251G>T