Canonical Allele Identifier: PA2827481501
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_001336267.1:p.Ala564Thr
CA2490866
NM_001349338.3:c.1690G>A