Canonical Allele Identifier: PA916006719
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 583038
ClinVar RCV Id: RCV000707263 RCV002469272 RCV002493251 RCV004026748
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230673.1:p.Met16Val
CA374340456
NM_001243744.2:c.46A>G