Canonical Allele Identifier: PA2580264576
Gene: FLG HGNC NCBI

Linked Data

ClinVar Variation Id: 2230756
ClinVar RCV Id: RCV002717769

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002007.1:p.Ala1888Pro
CA1105659
NM_002016.2:c.5662G>C