Canonical Allele Identifier: PA2580264660
Gene: FLG HGNC NCBI

Linked Data

ClinVar Variation Id: 2282913
ClinVar RCV Id: RCV002840396

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002007.1:p.Asp2046Asn
CA342057451
NM_002016.2:c.6136G>A