Canonical Allele Identifier: PA2827243314
Gene: FANCB HGNC NCBI

Linked Data

ClinVar Variation Id: 526482

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311091.1:p.Gly88Arg
CA10353219
NM_001324162.2:c.262G>A
CA412444913
NM_001324162.2:c.262G>C