Canonical Allele Identifier: PA2499260116
Gene: FLG HGNC NCBI

Linked Data

ClinVar Variation Id: 1272269
ClinVar RCV Id: RCV001686425

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002007.1:p.Gly1966Ser
CA1105526
NM_002016.2:c.5896G>A