Canonical Allele Identifier: PA2828919188
Gene: FGB HGNC NCBI
ClinVar RCV:
RCV000017815
ClinVar Variation:
16389
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369694.1:p.Leu383Arg
CA126442
NM_001382765.1:c.1148T>G