Canonical Allele Identifier: PA916006574
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 571161
ClinVar RCV Id: RCV000692215 RCV002388236 RCV003322809 RCV002060874
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.Arg488Ser
CA374105777
NM_001243743.2:c.1464G>T
CA374105780
NM_001243743.2:c.1464G>C