Canonical Allele Identifier: PA2827483292
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_001336270.1:p.Leu413Val
CA76530288
NM_001349341.3:c.1237C>G