Canonical Allele Identifier: PA2825578738
Gene: FANCL HGNC NCBI

Linked Data

ClinVar Variation Id: 1378618
ClinVar RCV Id: RCV001890201
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001108108.1:p.Pro365Ala
CA1670316
NM_001114636.1:c.1093C>G