Canonical Allele Identifier: PA2826330413
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 1729701
ClinVar RCV Id: RCV003151403 RCV002325052
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.Lys109Asn
CA374339221
NM_001243743.2:c.327A>T
CA374339222
NM_001243743.2:c.327A>C