Canonical Allele Identifier: PA658660864
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 449977
ClinVar RCV Id: RCV000523904 RCV000563212
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Ala516Phe
CA658657887
NM_000136.3:c.1546_1547delinsTT