Canonical Allele Identifier: PA2829372067
Gene: FLG HGNC NCBI

Linked Data

ClinVar Variation Id: 3095474
ClinVar RCV Id: RCV004386792

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002007.1:p.Ala1149Val
CA342083285
NM_002016.2:c.3446C>T