Canonical Allele Identifier: PA2828918933
Gene: FGB HGNC NCBI

Linked Data

ClinVar Variation Id: 2078262
ClinVar RCV Id: RCV002988540
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369691.1:p.Met297Ile
CA3114738
NM_001382762.1:c.891G>A
CA358515444
NM_001382762.1:c.891G>C
CA358515446
NM_001382762.1:c.891G>T