Canonical Allele Identifier: PA2826329917
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 127529
ClinVar RCV Id: RCV000115339 RCV000630863 RCV001030468 RCV001009634
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.Arg334Gln
CA287178
NM_001243743.2:c.1001G>A