Canonical Allele Identifier: PA299186
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 182485
ClinVar RCV Id: RCV000160486 RCV000477242 RCV000570128 RCV001273988 RCV001358089
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Glu417Lys
CA299184
NM_000136.3:c.1249G>A