Canonical Allele Identifier: PA2825204063
Gene: FGG HGNC NCBI

Linked Data

ClinVar Variation Id: 432325
ClinVar RCV Id: RCV000497584
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000500.2:p.Lys238Arg
CA358536471
NM_000509.5:c.713A>G