Canonical Allele Identifier: PA2499260149
Gene: FLG HGNC NCBI

Linked Data

ClinVar Variation Id: 1198208
ClinVar RCV Id: RCV001562294

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002007.1:p.Val2418Met
CA1104827
NM_002016.2:c.7252G>A