ClinGen Allele Registry
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Canonical Allele Identifier:
PA2830059819
Gene: C19orf12
HGNC
NCBI
Linked Data
ClinVar Variation Id:
1682823
ClinVar RCV Id:
RCV002237729
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_113636.2:p.Thr102Met
CA9351891
NM_031448.6:c.305C>T