Canonical Allele Identifier: PA658660880
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 485551
ClinVar RCV Id: RCV000567655 RCV000630828 RCV002293461
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Pro541Leu
CA374104406
NM_000136.3:c.1622C>T