Canonical Allele Identifier: PA2499299026
Gene: FANCB HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689846.1:p.Tyr720Cys
CA10352961
NM_152633.4:c.2159A>G