Canonical Allele Identifier: PA2826888300
Gene: TMEM143 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

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