Canonical Allele Identifier: PA2580176552
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 1765035
ClinVar RCV Id: RCV002376044
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230673.1:p.Thr30Ser
CA5137839
NM_001243744.2:c.88A>T
CA374340357
NM_001243744.2:c.89C>G