ClinGen Allele Registry
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Canonical Allele Identifier:
PA2827293395
Gene: TMEM138
HGNC
NCBI
Linked Data
ClinVar RCV:
RCV000407594
ClinVar Variation:
305067
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001317210.1:p.Arg103Gln
CA6034671
NM_001330281.2:c.308G>A