Canonical Allele Identifier: PA2580265191
Gene: FLG HGNC NCBI

Linked Data

ClinVar Variation Id: 2370646
ClinVar RCV Id: RCV002981955

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002007.1:p.Ser3271Tyr
CA1103663
NM_002016.2:c.9812C>A