Canonical Allele Identifier: PA2829372086
Gene: FLG HGNC NCBI

Linked Data

ClinVar Variation Id: 3095479
ClinVar RCV Id: RCV004386797

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002007.1:p.Gln1272His
CA1106501
NM_002016.2:c.3816G>C
CA342080961
NM_002016.2:c.3816G>T