ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2825055393
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_000127.2:p.Ile143Met
CA5137749
NM_000136.3:c.429A>G