Canonical Allele Identifier: PA2829372293
Gene: FLG HGNC NCBI

Linked Data

ClinVar Variation Id: 3095517
ClinVar RCV Id: RCV004386835

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002007.1:p.Arg2086His
CA1105334
NM_002016.2:c.6257G>A