Canonical Allele Identifier: PA2499260089
Gene: FLG HGNC NCBI

Linked Data

ClinVar Variation Id: 1206128
ClinVar RCV Id: RCV001573346

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002007.1:p.Arg1474Gln
CA1106231
NM_002016.2:c.4421G>A