Canonical Allele Identifier: PA916006772
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 656772
ClinVar RCV Id: RCV000813273
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230673.1:p.Phe44Ser
CA374340265
NM_001243744.2:c.131T>C