Canonical Allele Identifier: PA2499260091
Gene: FLG HGNC NCBI

Linked Data

ClinVar Variation Id: 1278160
ClinVar RCV Id: RCV001694901

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002007.1:p.Asp1484Glu
CA1106217
NM_002016.2:c.4452C>G
CA342074012
NM_002016.2:c.4452C>A