Canonical Allele Identifier: PA2573186608
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 1370031
ClinVar RCV Id: RCV001870914 RCV002388733
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.Ile487Met
CA374105800
NM_001243743.2:c.1461C>G