Canonical Allele Identifier: PA2829372373
Gene: FLG HGNC NCBI

Linked Data

ClinVar Variation Id: 3095541
ClinVar RCV Id: RCV004386859
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002007.1:p.Ser2399Pro
CA342048200
NM_002016.2:c.7195T>C