Canonical Allele Identifier: PA2499260124
Gene: FLG HGNC NCBI

Linked Data

ClinVar Variation Id: 1229450
ClinVar RCV Id: RCV001609690
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002007.1:p.Ala2076Thr
CA1105358
NM_002016.2:c.6226G>A