Canonical Allele Identifier: PA2741888108
Gene: FLG HGNC NCBI

Linked Data

ClinVar Variation Id: 2590356
ClinVar RCV Id: RCV003365825
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002007.1:p.Val1395Ala
CA1106338
NM_002016.2:c.4184T>C