ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2828918801
Gene: FGB
HGNC
NCBI
Linked Data
ClinVar Variation Id:
16385
ClinVar RCV Id:
RCV000017809
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001369690.1:p.Gly45Cys
CA126437
NM_001382761.1:c.133G>T