Canonical Allele Identifier: PA2580264251
Gene: FLG HGNC NCBI

Linked Data

ClinVar Variation Id: 2318916
ClinVar RCV Id: RCV002888887
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002007.1:p.Gly815Ala
CA342089632
NM_002016.2:c.2444G>C