Canonical Allele Identifier: PA2829372572
Gene: FLG HGNC NCBI

Linked Data

ClinVar Variation Id: 3095392
ClinVar RCV Id: RCV004386710

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002007.1:p.Arg3375Leu
CA1103528
NM_002016.2:c.10124G>T