Canonical Allele Identifier: PA2741888097
Gene: FLG HGNC NCBI

Linked Data

ClinVar Variation Id: 2639297
ClinVar RCV Id: RCV003408991
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002007.1:p.His1146Asn
CA1106683
NM_002016.2:c.3436C>A