Canonical Allele Identifier: PA645429957
Gene: FANCB HGNC NCBI

Linked Data

ClinVar Variation Id: 435140
ClinVar RCV Id: RCV000501276 RCV001516277 RCV003237883
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001018123.1:p.Leu43Ile
CA10353231
NM_001018113.2:c.127T>A