Canonical Allele Identifier: PA2573215797
Gene: FANCL HGNC NCBI

Linked Data

ClinVar Variation Id: 1440583

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361544.1:p.Pro375Thr
CA346930972
NM_001374615.1:c.1123C>A