Canonical Allele Identifier: PA2829872982
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_060532.2:p.Leu346del
CA1670325
NM_018062.4:c.1036_1038del