Canonical Allele Identifier: PA891845119
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 568009
ClinVar RCV Id: RCV000688242 RCV002331340
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Tyr146Ser
CA374338733
NM_000136.3:c.437A>C