Canonical Allele Identifier: PA2580264342
Gene: FLG HGNC NCBI

Linked Data

ClinVar Variation Id: 2290549
ClinVar RCV Id: RCV002854466

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002007.1:p.Gly1108Ala
CA342084203
NM_002016.2:c.3323G>C