Canonical Allele Identifier: PA2499260065
Gene: FLG HGNC NCBI

Linked Data

ClinVar Variation Id: 1264247
ClinVar RCV Id: RCV001667782

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002007.1:p.Ser847Thr
CA1107120
NM_002016.2:c.2539T>A