Canonical Allele Identifier: PA2827243680
Gene: FANCB HGNC NCBI

Linked Data

ClinVar Variation Id: 435139
ClinVar RCV Id: RCV000504138 RCV001857097
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311091.1:p.Phe743Cys
CA10352937
NM_001324162.2:c.2228T>G