Canonical Allele Identifier: PA645429958
Gene: FANCB HGNC NCBI

Linked Data

ClinVar Variation Id: 246614
ClinVar RCV Id: RCV000235722
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001018123.1:p.Cys79Arg
CA10584657
NM_001018113.2:c.235T>C