Canonical Allele Identifier: PA2580264586
Gene: FLG HGNC NCBI

Linked Data

ClinVar Variation Id: 2389518

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002007.1:p.Val1900Ala
CA1105640
NM_002016.2:c.5699T>C