Canonical Allele Identifier: PA2826888275
Gene: TMEM143 HGNC NCBI
ClinVar RCV:
RCV004183326
ClinVar Variation:
2341428
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001290467.1:p.Asp268Asn
CA9549455
NM_001303538.2:c.802G>A