Canonical Allele Identifier: PA658660745
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 456149
ClinVar RCV Id: RCV000549299 RCV002384041
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Thr344Ala
CA374108173
NM_000136.3:c.1030A>G