Canonical Allele Identifier: PA2499260147
Gene: FLG HGNC NCBI

Linked Data

ClinVar Variation Id: 1239802

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002007.1:p.Glu2398Gln
CA1104863
NM_002016.2:c.7192G>C