Canonical Allele Identifier: PA2825578487
Gene: FANCL HGNC NCBI

Linked Data

ClinVar Variation Id: 456243

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001108108.1:p.Arg68Pro
CA1670757
NM_001114636.1:c.203G>C