Canonical Allele Identifier: PA2829371973
Gene: FLG HGNC NCBI

Linked Data

ClinVar Variation Id: 3095454
ClinVar RCV Id: RCV004386772

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002007.1:p.Ser860Pro
CA342088355
NM_002016.2:c.2578T>C