Canonical Allele Identifier: PA2741888277
Gene: FLG HGNC NCBI

Linked Data

ClinVar Variation Id: 2639238
ClinVar RCV Id: RCV003408932

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002007.1:p.Arg3402Trp
CA1103479
NM_002016.2:c.10204C>T