Canonical Allele Identifier: PA916006567
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 819147
ClinVar RCV Id: RCV001011440 RCV001273979
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.Gln473Arg
CA374106032
NM_001243743.2:c.1418A>G