Canonical Allele Identifier: PA2580265270
Gene: FLG HGNC NCBI

Linked Data

ClinVar Variation Id: 2353537
ClinVar RCV Id: RCV002969259
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002007.1:p.Arg3445Ser
CA1103408
NM_002016.2:c.10335G>C
CA342070845
NM_002016.2:c.10335G>T