Canonical Allele Identifier: PA2827485797
Gene: FOXP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2705060
ClinVar RCV Id: RCV003575242
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336273.1:p.Lys341_Tyr342dup
CA1373976710
NM_001349344.3:c.1023_1028dup