Canonical Allele Identifier: PA201484
Gene: FOXP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 55847

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_116071.2:p.Pro568Ser
CA201483
NM_032682.6:c.1702C>T