Canonical Allele Identifier: PA2826888318
Gene: TMEM143 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001290468.1:p.Asp238Asn
CA9549455
NM_001303539.2:c.712G>A