Canonical Allele Identifier: PA2829372054
Gene: FLG HGNC NCBI

Linked Data

ClinVar Variation Id: 3095470
ClinVar RCV Id: RCV004386788

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002007.1:p.Arg1110Thr
CA1106732
NM_002016.2:c.3329G>C