Canonical Allele Identifier: PA2829372295
Gene: FLG HGNC NCBI

Linked Data

ClinVar Variation Id: 3095518
ClinVar RCV Id: RCV004386836
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002007.1:p.Ser2087Pro
CA342054841
NM_002016.2:c.6259T>C