Canonical Allele Identifier: PA916051528
Gene: FANCB HGNC NCBI
ClinVar RCV:
RCV000235722
ClinVar Variation:
246614
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689846.1:p.Cys79Arg
CA10584657
NM_152633.4:c.235T>C