Canonical Allele Identifier: PA2829372590
Gene: FLG HGNC NCBI

Linked Data

ClinVar Variation Id: 3095395
ClinVar RCV Id: RCV004386713

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002007.1:p.His3414Gln
CA1103455
NM_002016.2:c.10242C>A
CA342072463
NM_002016.2:c.10242C>G