Canonical Allele Identifier: PA2825056114
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 2585989
ClinVar RCV Id: RCV003368128
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Pro482Leu
CA374105883
NM_000136.3:c.1445C>T