Canonical Allele Identifier: PA170754
Gene: FGG HGNC NCBI

Linked Data

ClinVar Variation Id: 156105
ClinVar RCV Id: RCV000144152 RCV001509237
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000500.2:p.Ser404Pro
CA170753
NM_000509.5:c.1210T>C