Canonical Allele Identifier: PA2829372365
Gene: FLG HGNC NCBI

Linked Data

ClinVar Variation Id: 3095538
ClinVar RCV Id: RCV004386856

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002007.1:p.Ser2358Asn
CA1104912
NM_002016.2:c.7073G>A