Canonical Allele Identifier: PA2826332602
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 3230361
ClinVar RCV Id: RCV004520512
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230673.1:p.Arg46Lys
CA5137830
NM_001243744.2:c.137G>A