Canonical Allele Identifier: PA2741888101
Gene: FLG HGNC NCBI

Linked Data

ClinVar Variation Id: 2593397
ClinVar RCV Id: RCV003358565
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002007.1:p.Thr1262Arg
CA1106511
NM_002016.2:c.3785C>G