Canonical Allele Identifier: PA645431567
Gene: FANCL HGNC NCBI

Linked Data

ClinVar Variation Id: 241253
ClinVar RCV Id: RCV000233098 RCV001820756 RCV003316291 RCV003955361
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001108108.1:p.Asp326Glu
CA1670371
NM_001114636.1:c.978T>A
CA346932952
NM_001114636.1:c.978T>G