Canonical Allele Identifier: PA658660568
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 485544
ClinVar RCV Id: RCV000630855 RCV000567484 RCV002476246 RCV001788294
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Arg179Gln
CA5137696
NM_000136.3:c.536G>A