Canonical Allele Identifier: PA299147
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 182472
ClinVar RCV Id: RCV000160473 RCV000470152 RCV000564307 RCV000988216 RCV002271426 RCV002492634
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Arg185Gln
CA299145
NM_000136.3:c.554G>A