Canonical Allele Identifier: PA2825204111
Gene: FGG HGNC NCBI

Linked Data

ClinVar Variation Id: 2884084
ClinVar RCV Id: RCV003724242

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000500.2:p.Gln425Lys
CA108774381
NM_000509.5:c.1273C>A