Canonical Allele Identifier: PA2827293395
Gene: TMEM138 HGNC NCBI
ClinVar RCV:
RCV000407594
ClinVar Variation:
305067
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317210.1:p.Arg103Gln
CA6034671
NM_001330281.2:c.308G>A