Canonical Allele Identifier: PA2829372347
Gene: FLG HGNC NCBI

Linked Data

ClinVar Variation Id: 3095532
ClinVar RCV Id: RCV004386850

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002007.1:p.His2305Arg
CA1104979
NM_002016.2:c.6914A>G