Canonical Allele Identifier: PA916006848
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 824862
ClinVar RCV Id: RCV001022419 RCV001276459
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230673.1:p.Pro147Thr
CA374338726
NM_001243744.2:c.439C>A