Canonical Allele Identifier: PA245992
Gene: FANCB HGNC NCBI

Linked Data

ClinVar Variation Id: 197705
ClinVar RCV Id: RCV000178817 RCV000865306 RCV001167815 RCV001167816 RCV002453636 RCV003436973
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001018123.1:p.Phe380Leu
CA245990
NM_001018113.2:c.1140T>A
CA412442885
NM_001018113.2:c.1140T>G
CA412442890
NM_001018113.2:c.1138T>C