Canonical Allele Identifier: PA2499260192
Gene: FLG HGNC NCBI

Linked Data

ClinVar Variation Id: 1205900
ClinVar RCV Id: RCV001572770

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002007.1:p.Asn3534Ser
CA1103263
NM_002016.2:c.10601A>G