Canonical Allele Identifier: PA658800487
Gene: FANCB HGNC NCBI

Linked Data

ClinVar Variation Id: 526482

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001018123.1:p.Gly88Arg
CA10353219
NM_001018113.2:c.262G>A
CA412444913
NM_001018113.2:c.262G>C