Canonical Allele Identifier: PA2580423125
Gene: TMEM143 HGNC NCBI

Linked Data

ClinVar Variation Id: 2272248
ClinVar RCV Id: RCV004125966
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060743.2:p.Thr142Met
CA9549628
NM_018273.4:c.425C>T