Canonical Allele Identifier: PA2826080729
Gene: FOXP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1765412
ClinVar RCV Id: RCV002376335
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001166238.1:p.Gly30Asp
CA369105680
NM_001172767.2:c.89G>A