Canonical Allele Identifier: PA2828919191
Gene: FGB HGNC NCBI

Linked Data

ClinVar Variation Id: 2078262
ClinVar RCV Id: RCV002988540
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369694.1:p.Met397Ile
CA3114738
NM_001382765.1:c.1191G>A
CA358515444
NM_001382765.1:c.1191G>C
CA358515446
NM_001382765.1:c.1191G>T