Canonical Allele Identifier: PA2828439839
Gene: FOXP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2062820
ClinVar RCV Id: RCV002958031
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357477.1:p.Leu314Val
CA76530288
NM_001370548.1:c.940C>G