Canonical Allele Identifier: PA2825329636
Gene: FANCB HGNC NCBI

Linked Data

ClinVar Variation Id: 840424
ClinVar RCV Id: RCV001042410

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001018123.1:p.Cys595Trp
CA412439629
NM_001018113.2:c.1785C>G