Canonical Allele Identifier: PA2825204104
Gene: FGG HGNC NCBI

Linked Data

ClinVar Variation Id: 2306997
ClinVar RCV Id: RCV002879331
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000500.2:p.Thr400Ser
CA108774410
NM_000509.5:c.1198A>T
CA358535346
NM_000509.5:c.1199C>G