Canonical Allele Identifier: PA2829371966
Gene: FLG HGNC NCBI

Linked Data

ClinVar Variation Id: 3095451
ClinVar RCV Id: RCV004386769

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002007.1:p.Gly854Glu
CA1107106
NM_002016.2:c.2561G>A