Canonical Allele Identifier: PA2828530062
Gene: FANCL HGNC NCBI

Linked Data

ClinVar Variation Id: 950949
ClinVar RCV Id: RCV001222772

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361544.1:p.Met89Ile
CA347034613
NM_001374615.1:c.267G>T
CA347034614
NM_001374615.1:c.267G>A
CA347034615
NM_001374615.1:c.267G>C