Canonical Allele Identifier: PA2580264577
Gene: FLG HGNC NCBI

Linked Data

ClinVar Variation Id: 2498416
ClinVar RCV Id: RCV003222625
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002007.1:p.Ser1889Thr
CA1105658
NM_002016.2:c.5665T>A