ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2580176641
Gene: FANCC
HGNC
NCBI
Linked Data
ClinVar Variation Id:
2446649
ClinVar RCV Id:
RCV003159479
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001230673.1:p.Ile143Met
CA5137749
NM_001243744.2:c.429A>G