Canonical Allele Identifier: PA645429958
Gene: FANCB HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001018123.1:p.Cys79Arg
CA10584657
NM_001018113.2:c.235T>C