Canonical Allele Identifier: PA2829372261
Gene: FLG HGNC NCBI

Linked Data

ClinVar Variation Id: 3095513
ClinVar RCV Id: RCV004386831

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002007.1:p.Tyr2039Ser
CA1105408
NM_002016.2:c.6116A>C