Canonical Allele Identifier: PA2825055998
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 1762512
ClinVar RCV Id: RCV002412511
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Thr420Lys
CA374107360
NM_000136.3:c.1259C>A