ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2573067767
Gene: FANCC
HGNC
NCBI
Linked Data
ClinVar Variation Id:
1300396
ClinVar RCV Id:
RCV001732365
RCV002343807
RCV002488492
RCV002539805
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001230673.1:p.Asn164Thr
CA196885560
NM_001243744.2:c.491A>C