Canonical Allele Identifier: PA2580264421
Gene: FLG HGNC NCBI

Linked Data

ClinVar Variation Id: 2315456
ClinVar RCV Id: RCV002919288

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002007.1:p.Gly1288Arg
CA1106481
NM_002016.2:c.3862G>C
CA342080703
NM_002016.2:c.3862G>A