Canonical Allele Identifier: PA2829372220
Gene: FLG HGNC NCBI

Linked Data

ClinVar Variation Id: 3095509
ClinVar RCV Id: RCV004386827

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002007.1:p.Ala1946Ser
CA30551727
NM_002016.2:c.5836G>T