Canonical Allele Identifier: PA2827243598
Gene: FANCB HGNC NCBI

Linked Data

ClinVar Variation Id: 246611
ClinVar RCV Id: RCV000292661 RCV000375315 RCV000437503 RCV001080424 RCV001269483 RCV000720996 RCV000990470 RCV001726070 RCV003907910
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311091.1:p.Phe590Ser
CA10353003
NM_001324162.2:c.1769T>C