Canonical Allele Identifier: PA916051655
Gene: FANCB HGNC NCBI

Linked Data

ClinVar Variation Id: 246613
ClinVar RCV Id: RCV000237072 RCV003947807 RCV001820789 RCV003884430
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689846.1:p.Pro697Leu
CA10352969
NM_152633.4:c.2090C>T