Canonical Allele Identifier: PA2573277733
Gene: FGG HGNC NCBI

Linked Data

ClinVar Variation Id: 1684485

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_068656.2:p.Thr397Ile
CA358535369
NM_021870.3:c.1190C>T