Canonical Allele Identifier: PA2826329916
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 216279
ClinVar RCV Id: RCV000195976 RCV000486496 RCV001009657 RCV001354801 RCV001818484
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.Arg334Trp
CA336089
NM_001243743.2:c.1000C>T