Canonical Allele Identifier: PA2580264425
Gene: FLG HGNC NCBI

Linked Data

ClinVar Variation Id: 2368110
ClinVar RCV Id: RCV002997118
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002007.1:p.Gln1313His
CA1106436
NM_002016.2:c.3939A>C
CA342080189
NM_002016.2:c.3939A>T