Canonical Allele Identifier: PA2827486001
Gene: FOXP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 55847

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336273.1:p.Pro467Ser
CA201483
NM_001349344.3:c.1399C>T