Canonical Allele Identifier: PA645429992
Gene: FANCB HGNC NCBI

Linked Data

ClinVar Variation Id: 408160
ClinVar RCV Id: RCV000766076 RCV001487463 RCV001821263 RCV003942481 RCV004022680
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001018123.1:p.Cys574Ser
CA10353010
NM_001018113.2:c.1720T>A
CA412439766
NM_001018113.2:c.1721G>C