Canonical Allele Identifier: PA1139694906
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 970441
ClinVar RCV Id: RCV001246013 RCV002379941 RCV002484373 RCV001586088
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230673.1:p.Gln437Arg
CA374107260
NM_001243744.2:c.1310A>G