Canonical Allele Identifier: PA2829371975
Gene: FLG HGNC NCBI

Linked Data

ClinVar Variation Id: 3095455
ClinVar RCV Id: RCV004386773

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002007.1:p.Ser876Pro
CA1107072
NM_002016.2:c.2626T>C