Canonical Allele Identifier: PA645429074
Gene: FANCE HGNC NCBI

Linked Data

ClinVar Variation Id: 356449

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_068741.1:p.Leu326Trp
CA3771571
NM_021922.3:c.977T>G