Canonical Allele Identifier: PA2580264847
Gene: FLG HGNC NCBI

Linked Data

ClinVar Variation Id: 2393730
ClinVar RCV Id: RCV002738676

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002007.1:p.Asp2377Glu
CA30549107
NM_002016.2:c.7131C>G
CA342049229
NM_002016.2:c.7131C>A