Canonical Allele Identifier: PA916051523
Gene: FANCB HGNC NCBI

Linked Data

ClinVar Variation Id: 435140

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689846.1:p.Leu43Ile
CA10353231
NM_152633.4:c.127T>A