Canonical Allele Identifier: PA2580264371
Gene: FLG HGNC NCBI

Linked Data

ClinVar Variation Id: 2290935
ClinVar RCV Id: RCV002859468

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002007.1:p.Arg1154Thr
CA1106664
NM_002016.2:c.3461G>C