Canonical Allele Identifier: PA2580264381
Gene: FLG HGNC NCBI

Linked Data

ClinVar Variation Id: 2382620
ClinVar RCV Id: RCV002684688

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002007.1:p.His1181Tyr
CA1106634
NM_002016.2:c.3541C>T