Canonical Allele Identifier: PA2499260077
Gene: FLG HGNC NCBI

Linked Data

ClinVar Variation Id: 1183066
ClinVar RCV Id: RCV001540830
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002007.1:p.Arg1140Gln
CA1106690
NM_002016.2:c.3419G>A