Canonical Allele Identifier: PA645389264
Gene: FOXP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 280463
ClinVar RCV Id: RCV000283441
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_116071.2:p.Tyr470Cys
CA2490997
NM_032682.6:c.1409A>G