Canonical Allele Identifier: PA2829372291
Gene: FLG HGNC NCBI

Linked Data

ClinVar Variation Id: 3095516
ClinVar RCV Id: RCV004386834
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002007.1:p.Ser2084Phe
CA1105338
NM_002016.2:c.6251C>T