Canonical Allele Identifier: PA2826888362
Gene: TMEM143 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001290469.1:p.His273Arg
CA9549371
NM_001303540.2:c.818A>G