Canonical Allele Identifier: PA2826333847
Gene: FOXP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1305023
ClinVar RCV Id: RCV001765198
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001231737.1:p.Pro413Ala
CA353493978
NM_001244808.3:c.1237C>G