Canonical Allele Identifier: PA2829371956
Gene: FLG HGNC NCBI

Linked Data

ClinVar Variation Id: 3095449
ClinVar RCV Id: RCV004386767

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002007.1:p.Ser803Pro
CA1107187
NM_002016.2:c.2407T>C