Canonical Allele Identifier: PA2573202015
Gene: TMEM138 HGNC NCBI

Linked Data

ClinVar Variation Id: 1401571
ClinVar RCV Id: RCV001912943
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317210.1:p.Arg45Cys
CA6034589
NM_001330281.2:c.133C>T