Canonical Allele Identifier: PA2741888075
Gene: FLG HGNC NCBI

Linked Data

ClinVar Variation Id: 2591148
ClinVar RCV Id: RCV003340448
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002007.1:p.Thr814Ala
CA1107169
NM_002016.2:c.2440A>G