Canonical Allele Identifier: PA2580264862
Gene: FLG HGNC NCBI

Linked Data

ClinVar Variation Id: 2255813
ClinVar RCV Id: RCV002772516
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002007.1:p.Arg2403Pro
CA1104855
NM_002016.2:c.7208G>C