Canonical Allele Identifier: PA2580265264
Gene: FLG HGNC NCBI

Linked Data

ClinVar Variation Id: 2384905
ClinVar RCV Id: RCV002675364

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002007.1:p.Asp3420Gly
CA1103445
NM_002016.2:c.10259A>G