Canonical Allele Identifier: PA126414
Gene: FGG HGNC NCBI

Linked Data

ClinVar Variation Id: 16374
ClinVar RCV Id: RCV000017796
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000500.2:p.Asp390His
CA126413
NM_000509.5:c.1168G>C