Canonical Allele Identifier: PA2499260110
Gene: FLG HGNC NCBI

Linked Data

ClinVar Variation Id: 1206956
ClinVar RCV Id: RCV001574778

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002007.1:p.Pro1908Ser
CA1105626
NM_002016.2:c.5722C>T