Canonical Allele Identifier: PA2826330074
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 1037722
ClinVar RCV Id: RCV001340915
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.Thr27Ser
CA374340377
NM_001243743.2:c.80C>G
CA374340380
NM_001243743.2:c.79A>T