Canonical Allele Identifier: PA2580264584
Gene: FLG HGNC NCBI

Linked Data

ClinVar Variation Id: 2389517
ClinVar RCV Id: RCV002709174
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002007.1:p.Val1900Leu
CA1105641
NM_002016.2:c.5698G>T
CA342061910
NM_002016.2:c.5698G>C