Canonical Allele Identifier: PA2580264373
Gene: FLG HGNC NCBI

Linked Data

ClinVar Variation Id: 2262339
ClinVar RCV Id: RCV002808222
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002007.1:p.Gly1161Ser
CA30557656
NM_002016.2:c.3481G>A