Canonical Allele Identifier: PA916006741
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 219747
ClinVar RCV Id: RCV000205596 RCV001017291 RCV001276598
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230673.1:p.His37Asp
CA349729
NM_001243744.2:c.109C>G