Canonical Allele Identifier: PA2499260064
Gene: FLG HGNC NCBI

Linked Data

ClinVar Variation Id: 1208753
ClinVar RCV Id: RCV001577188
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002007.1:p.Ser805Phe
CA1107185
NM_002016.2:c.2414C>T