Canonical Allele Identifier: PA2826331667
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 1468966
ClinVar RCV Id: RCV001961333 RCV002423167 RCV002492174
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.Pro418Ser
CA374107371
NM_001243743.2:c.1252C>T