Canonical Allele Identifier: PA2827485859
Gene: FOXP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 873452
ClinVar RCV Id: RCV001095670
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336273.1:p.Tyr369Phe
CA353493237
NM_001349344.3:c.1106A>T