Canonical Allele Identifier: PA916051574
Gene: FANCB HGNC NCBI
ClinVar RCV:
RCV000548316
ClinVar Variation:
456175
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689846.1:p.Thr360Met
CA10353134
NM_152633.4:c.1079C>T