Canonical Allele Identifier: PA109157
Gene: FGG HGNC NCBI

Linked Data

ClinVar Variation Id: 2572634
ClinVar RCV Id: RCV003314519

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_068656.2:p.Arg401Trp
CA108774405
NM_021870.3:c.1201C>T