Canonical Allele Identifier: PA126395
Gene: FGG HGNC NCBI

Linked Data

ClinVar Variation Id: 16364
ClinVar RCV Id: RCV000017784
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000500.2:p.Asn334Lys
CA358535820
NM_000509.5:c.1002T>G
CA358535821
NM_000509.5:c.1002T>A