Canonical Allele Identifier: PA658662263
Gene: FANCB HGNC NCBI

Linked Data

ClinVar Variation Id: 456186
ClinVar RCV Id: RCV000532263
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001018123.1:p.Tyr18His
CA327063415
NM_001018113.2:c.52T>C