Canonical Allele Identifier: PA645402365
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 421810
ClinVar RCV Id: RCV000482048 RCV001835817 RCV003168961
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Val117Ile
CA5137757
NM_000136.3:c.349G>A