Canonical Allele Identifier: PA2826337207
Gene: FOXP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1422778

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001231744.2:p.Ala312Thr
CA2491051
NM_001244815.2:c.934G>A