Canonical Allele Identifier: PA916006838
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 220563
ClinVar RCV Id: RCV000204465 RCV002327064
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230673.1:p.Pro142Ala
CA348683
NM_001243744.2:c.424C>G