Canonical Allele Identifier: PA916051703
Gene: FANCB HGNC NCBI

Linked Data

ClinVar Variation Id: 246615

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689846.1:p.Arg818Gly
CA10352912
NM_152633.4:c.2452A>G