Canonical Allele Identifier: PA2827484399
Gene: FOXP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 55847

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336271.1:p.Pro468Ser
CA201483
NM_001349342.3:c.1402C>T