Canonical Allele Identifier: PA126404
Gene: FGG HGNC NCBI

Linked Data

ClinVar Variation Id: 16368
ClinVar RCV Id: RCV000017788
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_068656.2:p.Gln355Arg
CA126402
NM_021870.3:c.1064A>G