Canonical Allele Identifier: PA2827243311
Gene: FANCB HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311091.1:p.Cys79Arg
CA10584657
NM_001324162.2:c.235T>C