Canonical Allele Identifier: PA2826335114
Gene: FOXP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 451160
ClinVar RCV Id: RCV000523347
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001231741.1:p.Ala374Thr
CA353493393
NM_001244812.1:c.1120G>A