Canonical Allele Identifier: PA2827485195
Gene: FOXP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2441549
ClinVar RCV Id: RCV003144090 RCV003778881
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336272.1:p.Ala463Thr
CA2490866
NM_001349343.3:c.1387G>A