Canonical Allele Identifier: PA2826888284
Gene: TMEM143 HGNC NCBI

Linked Data

ClinVar Variation Id: 3178814
ClinVar RCV Id: RCV004475186
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001290467.1:p.His338Arg
CA9549371
NM_001303538.2:c.1013A>G