Canonical Allele Identifier: PA916051622
Gene: FANCB HGNC NCBI

Linked Data

ClinVar Variation Id: 281375
ClinVar RCV Id: RCV000514485 RCV001087773 RCV002518813 RCV003947831
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689846.1:p.Thr553Met
CA10353018
NM_152633.4:c.1658C>T