Canonical Allele Identifier: PA2499260078
Gene: FLG HGNC NCBI

Linked Data

ClinVar Variation Id: 1206279
ClinVar RCV Id: RCV001573733

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002007.1:p.Glu1147Gly
CA1106678
NM_002016.2:c.3440A>G