Canonical Allele Identifier: PA2825329637
Gene: FANCB HGNC NCBI

Linked Data

ClinVar Variation Id: 2811337
ClinVar RCV Id: RCV003637058
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001018123.1:p.Thr596Asn
CA412439625
NM_001018113.2:c.1787C>A