ClinGen Allele Registry
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Canonical Allele Identifier:
PA2825811555
Gene: FAM111B
HGNC
NCBI
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001136175.1:p.Arg597Gly
CA150786
NM_001142703.1:c.1789A>G