ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA126433
Gene: FGB
HGNC
NCBI
Linked Data
ClinVar Variation Id:
16383
ClinVar RCV Id:
RCV000017807
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_005132.2:p.Ala365Thr
CA126431
NM_005141.5:c.1093G>A