Allele Registry

Canonical Allele Identifier: PA645430002

Gene: FANCB HGNC NCBI

ClinVar Allele:

430667

ClinVar RCV:

RCV000504138

RCV001857097

ClinVar Variation:

435139

HGVS (amino-acid)	Matching Registered Transcripts
NP_001018123.1:p.Phe743Cys	CA10352937 NM_001018113.2:c.2228T>G