ClinGen Allele Registry
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Canonical Allele Identifier:
PA916006882
Gene: FANCC
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000567484
RCV000630855
RCV001788294
RCV002476246
ClinVar Variation:
485544
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001230673.1:p.Arg179Gln
CA5137696
NM_001243744.2:c.536G>A