Canonical Allele Identifier: PA2741960733
Gene: FANCL HGNC NCBI

Linked Data

ClinVar Variation Id: 2765449
ClinVar RCV Id: RCV003522640

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060532.2:p.Ser77Pro
CA347034702
NM_018062.4:c.229T>C