Canonical Allele Identifier: PA2827480304
Gene: FOXP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 280463
ClinVar RCV Id: RCV000283441

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336266.2:p.Tyr369Cys
CA2490997
NM_001349337.2:c.1106A>G