Canonical Allele Identifier: PA2825329692
Gene: FANCB HGNC NCBI

Linked Data

ClinVar Variation Id: 1023841
ClinVar RCV Id: RCV001323948
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001018123.1:p.Tyr720Cys
CA10352961
NM_001018113.2:c.2159A>G