Canonical Allele Identifier: PA2829372271
Gene: FLG HGNC NCBI

Linked Data

ClinVar Variation Id: 3095514
ClinVar RCV Id: RCV004386832

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002007.1:p.Gln2069Lys
CA1105373
NM_002016.2:c.6205C>A