Canonical Allele Identifier: PA2829372100
Gene: FLG HGNC NCBI

Linked Data

ClinVar Variation Id: 3095483
ClinVar RCV Id: RCV004386801

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002007.1:p.His1339Arg
CA1106400
NM_002016.2:c.4016A>G