Canonical Allele Identifier: PA2827481503
Gene: FOXP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 55847

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336267.1:p.Pro568Ser
CA201483
NM_001349338.3:c.1702C>T