Canonical Allele Identifier: PA2829372072
Gene: FLG HGNC NCBI

Linked Data

ClinVar Variation Id: 3095477
ClinVar RCV Id: RCV004386795

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002007.1:p.His1168Gln
CA1106649
NM_002016.2:c.3504C>G
CA342082853
NM_002016.2:c.3504C>A