Canonical Allele Identifier: PA299214
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 182495
ClinVar RCV Id: RCV000160497 RCV002426792 RCV002484995 RCV001831983
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Ile80Thr
CA299212
NM_000136.3:c.239T>C