Canonical Allele Identifier: PA2825056172
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 1774713
ClinVar RCV Id: RCV002403037
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Met512Thr
CA374104867
NM_000136.3:c.1535T>C