Canonical Allele Identifier: PA2580264426
Gene: FLG HGNC NCBI

Linked Data

ClinVar Variation Id: 2229984
ClinVar RCV Id: RCV002717419

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002007.1:p.Asp1324Glu
CA1106419
NM_002016.2:c.3972C>A
CA342079995
NM_002016.2:c.3972C>G