Canonical Allele Identifier: PA645430009
Gene: FANCB HGNC NCBI

Linked Data

ClinVar Variation Id: 246615
ClinVar RCV Id: RCV000236537 RCV000301708 RCV000390121 RCV000502067 RCV003947808 RCV003437033
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001018123.1:p.Arg818Gly
CA10352912
NM_001018113.2:c.2452A>G