Canonical Allele Identifier: PA126398
Gene: FGG HGNC NCBI

Linked Data

ClinVar Variation Id: 16365
ClinVar RCV Id: RCV000017785 RCV002513087
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_068656.2:p.Asn334Ile
CA126396
NM_021870.3:c.1001A>T