Canonical Allele Identifier: PA916006780
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 409659
ClinVar RCV Id: RCV000469467 RCV002402274
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230673.1:p.Leu52Phe
CA16612741
NM_001243744.2:c.156G>C
CA374340206
NM_001243744.2:c.156G>T