Canonical Allele Identifier: PA2825578739
Gene: FANCL HGNC NCBI

Linked Data

ClinVar Variation Id: 1440583

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001108108.1:p.Pro365Thr
CA346930972
NM_001114636.1:c.1093C>A