Canonical Allele Identifier: PA2825578729
Gene: FANCL HGNC NCBI

Linked Data

ClinVar Variation Id: 2039117
ClinVar RCV Id: RCV002907801
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001108108.1:p.Leu351del
CA1670325
NM_001114636.1:c.1051_1053del