ClinGen Allele Registry
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Canonical Allele Identifier:
PA2827075602
Gene: FAM168B
HGNC
NCBI
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001308673.1:p.Leu161Met
CA348528300
NM_001321744.1:c.481C>A