Canonical Allele Identifier: PA645429990
Gene: FANCB HGNC NCBI

Linked Data

ClinVar Variation Id: 368024
ClinVar RCV Id: RCV000331306 RCV000388194 RCV000500090 RCV002392931 RCV002488832 RCV000524700
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001018123.1:p.Lys498Asn
CA10353043
NM_001018113.2:c.1494G>T
CA412441186
NM_001018113.2:c.1494G>C