Canonical Allele Identifier: PA126394
Gene: FGG HGNC NCBI

Linked Data

ClinVar Variation Id: 16363
ClinVar RCV Id: RCV000017783 RCV003944828
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000500.2:p.Gly318Val
CA126393
NM_000509.5:c.953G>T