Canonical Allele Identifier: PA645430002
Gene: FANCB HGNC NCBI

Linked Data

ClinVar Variation Id: 435139
ClinVar RCV Id: RCV000504138 RCV001857097
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Amino-acid Alleles

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