Canonical Allele Identifier: PA2829372369
Gene: FLG HGNC NCBI

Linked Data

ClinVar Variation Id: 3095540
ClinVar RCV Id: RCV004386858
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002007.1:p.Ser2371Thr
CA342049270
NM_002016.2:c.7112G>C