Canonical Allele Identifier: PA916051528
Gene: FANCB HGNC NCBI

Linked Data

ClinVar Variation Id: 246614
ClinVar RCV Id: RCV000235722

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689846.1:p.Cys79Arg
CA10584657
NM_152633.4:c.235T>C