Allele Registry

Canonical Allele Identifier: PA109157

Gene: FGG HGNC NCBI

ClinVar RCV:

RCV003314519

ClinVar Variation:

2572634

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