Canonical Allele Identifier: PA2829372250
Gene: FLG HGNC NCBI

Linked Data

ClinVar Variation Id: 3095512
ClinVar RCV Id: RCV004386830

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002007.1:p.Ala2014Pro
CA342058430
NM_002016.2:c.6040G>C