Canonical Allele Identifier: PA2580264671
Gene: FLG HGNC NCBI

Linked Data

ClinVar Variation Id: 2374643
ClinVar RCV Id: RCV003012712

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002007.1:p.Phe2090Leu
CA1105328
NM_002016.2:c.6270C>A
CA342054720
NM_002016.2:c.6270C>G
CA342054752
NM_002016.2:c.6268T>C