Canonical Allele Identifier: PA2830289268
Gene: FOXP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 235442
ClinVar RCV Id: RCV000224051 RCV000361651
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_683697.2:p.Ala425Val
CA4446041
NM_148899.3:c.1274C>T