Canonical Allele Identifier: PA658831698
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_055306.1:p.Tyr531His
CA10584037
NM_014491.4:c.1591T>C