Canonical Allele Identifier: PA658800370
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 526329
ClinVar RCV Id: RCV000630844 RCV001354482 RCV003302983
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Ile523Thr
CA374104701
NM_000136.3:c.1568T>C