Canonical Allele Identifier: PA2830289135
Gene: FOXP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 195296
ClinVar RCV Id: RCV000175859 RCV000234933 RCV002336427 RCV003927612
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_683697.2:p.Gln17Leu
CA241662
NM_148899.3:c.50A>T