Canonical Allele Identifier: PA2826330067
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 134301
ClinVar RCV Id: RCV000120974 RCV000513630 RCV000573438 RCV000988227 RCV001083879 RCV001168031 RCV001357504 RCV003891642
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.Ser26Phe
CA159399
NM_001243743.2:c.77C>T