Canonical Allele Identifier: PA2573256981
Gene: FOXP3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1354456
ClinVar RCV Id: RCV001866434

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_054728.2:p.Arg369His
CA10411663
NM_014009.4:c.1106G>A