Canonical Allele Identifier: PA2741888102
Gene: FLG HGNC NCBI

Linked Data

ClinVar Variation Id: 2639293
ClinVar RCV Id: RCV003408987

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002007.1:p.Glu1277Gln
CA1106496
NM_002016.2:c.3829G>C