Canonical Allele Identifier: PA916051530
Gene: FANCB HGNC NCBI

Linked Data

ClinVar Variation Id: 526482

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689846.1:p.Gly88Arg
CA10353219
NM_152633.4:c.262G>A
CA412444913
NM_152633.4:c.262G>C