Canonical Allele Identifier: PA2825055692
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 1040691
ClinVar RCV Id: RCV001344376 RCV002431968
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Cys274Ser
CA196562479
NM_000136.3:c.820T>A
CA374109215
NM_000136.3:c.821G>C