Canonical Allele Identifier: PA2580264654
Gene: FLG HGNC NCBI

Linked Data

ClinVar Variation Id: 2292483
ClinVar RCV Id: RCV002832497

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002007.1:p.Gly2023Trp
CA1105431
NM_002016.2:c.6067G>T