ClinGen Allele Registry
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Canonical Allele Identifier:
PA2826672383
Gene: TMEM139
HGNC
NCBI
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001269806.1:p.Pro13Leu
CA369654108
NM_001282877.1:c.38C>T