Canonical Allele Identifier: PA2826329841
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 3230388
ClinVar RCV Id: RCV004520539
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.Ala181Ser
CA374109845
NM_001243743.2:c.541G>T