Canonical Allele Identifier: PA2499260123
Gene: FLG HGNC NCBI

Linked Data

ClinVar Variation Id: 1183365
ClinVar RCV Id: RCV001541191
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002007.1:p.Glu2074Gln
CA1105363
NM_002016.2:c.6220G>C