Canonical Allele Identifier: PA2826888300
Gene: TMEM143 HGNC NCBI

Linked Data

ClinVar Variation Id: 3178817
ClinVar RCV Id: RCV004475189
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001290468.1:p.Ser92Leu
CA9549680
NM_001303539.2:c.275C>T