Canonical Allele Identifier: PA2499260079
Gene: FLG HGNC NCBI

Linked Data

ClinVar Variation Id: 1298018

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002007.1:p.Ala1167Gly
CA1106651
NM_002016.2:c.3500C>G