Canonical Allele Identifier: PA2580264642
Gene: FLG HGNC NCBI

Linked Data

ClinVar Variation Id: 2221655
ClinVar RCV Id: RCV002683149
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002007.1:p.Ala1991Val
CA1105477
NM_002016.2:c.5972C>T