Canonical Allele Identifier: PA2580430761
Gene: FGG HGNC NCBI

Linked Data

ClinVar Variation Id: 2211603
ClinVar RCV Id: RCV002669039

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_068656.2:p.Ala383Pro
CA108774421
NM_021870.3:c.1147G>C