ClinGen Allele Registry
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Canonical Allele Identifier:
PA186056
Gene: C19orf12
HGNC
NCBI
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Transcript change
NP_001242976.1:p.Gly42Arg
NM_001256047.2:c.124G>A
NM_001256047.2:c.124G>C