Canonical Allele Identifier: PA2580264667
Gene: FLG HGNC NCBI

Linked Data

ClinVar Variation Id: 2363624
ClinVar RCV Id: RCV002990228

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002007.1:p.Arg2077Cys
CA1105356
NM_002016.2:c.6229C>T