Canonical Allele Identifier: PA916006694
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 422569
ClinVar RCV Id: RCV000481288
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230673.1:p.Val6Leu
CA16618897
NM_001243744.2:c.16G>C
CA374340519
NM_001243744.2:c.16G>T