Canonical Allele Identifier: PA2741888264
Gene: FLG HGNC NCBI

Linked Data

ClinVar Variation Id: 2639245
ClinVar RCV Id: RCV003408939

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002007.1:p.Arg3270His
CA1103665
NM_002016.2:c.9809G>A