Canonical Allele Identifier: PA2826338101
Gene: FOXP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1422778

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001231745.1:p.Ala412Thr
CA2491051
NM_001244816.1:c.1234G>A