Canonical Allele Identifier: PA2499260112
Gene: FLG HGNC NCBI

Linked Data

ClinVar Variation Id: 1175489
ClinVar RCV Id: RCV001530664
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002007.1:p.Asn1913His
CA1105617
NM_002016.2:c.5737A>C