Canonical Allele Identifier: PA2826080650
Gene: FOXP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 242975
ClinVar RCV Id: RCV000234952
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001166237.1:p.Tyr530His
CA10584037
NM_001172766.3:c.1588T>C