Canonical Allele Identifier: PA2826330509
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 1218708
ClinVar RCV Id: RCV001593904 RCV002324158 RCV002573357
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.Gln136Pro
CA374338794
NM_001243743.2:c.407A>C