Canonical Allele Identifier: PA2580176484
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 1774685
ClinVar RCV Id: RCV002403014
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.Met512Val
CA374104870
NM_001243743.2:c.1534A>G