ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA916006823
Gene: FANCC
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar Allele:
407764
ClinVar RCV:
RCV000482048
RCV001835817
RCV003168961
ClinVar Variation:
421810
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001230673.1:p.Val117Ile
CA5137757
NM_001243744.2:c.349G>A