Canonical Allele Identifier: PA2580265238
Gene: FLG HGNC NCBI

Linked Data

ClinVar Variation Id: 2367393
ClinVar RCV Id: RCV002984748

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002007.1:p.Gln3308Leu
CA1103620
NM_002016.2:c.9923A>T