Canonical Allele Identifier: PA645482454
Gene: FOXP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 235442
ClinVar RCV Id: RCV000224051 RCV000361651
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001166238.1:p.Ala450Val
CA4446041
NM_001172767.2:c.1349C>T