Canonical Allele Identifier: PA2499242501
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 1052139
ClinVar RCV Id: RCV001360267 RCV002357221
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230673.1:p.Met406Thr
CA374107448
NM_001243744.2:c.1217T>C