Canonical Allele Identifier: PA2580264400
Gene: FLG HGNC NCBI

Linked Data

ClinVar Variation Id: 2227870
ClinVar RCV Id: RCV002702600

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002007.1:p.His1232Asn
CA1106554
NM_002016.2:c.3694C>A